Patent Grant
9868988
Transplantation of organs has progressed from a risky experimental therapy to a safe and life-saving treatment modality in a relatively short span of five decades. However, transplant recipients require life-long treatment with non-specific, toxic, and multiple immunosuppressive drugs, and are ever under the threat of losing their allografts because of immune rejection of the transplanted organ.
Acute rejection of an organ transplanted from one human to another is an important risk factor for allograft failure. The outcome of acute rejection is, however, difficult to predict.
Currently, observation of histologic features in allograft tissue obtained by core needle biopsy is the best predictor whether an acute rejection will respond to anti-rejection therapy. However, the invasive procedure of allograft biopsy is associated with complications such as bleeding, arteriovenous fistula, and even graft loss. Thus, there is a need for a non-invasive method for determining whether a patient suffering from acute rejection of a transplant organ is at risk of loss of the transplanted organ.
The above need has been met by the present invention, which provides in one aspect, a method for assessing risk of organ rejection in a patient having a transplanted organ. The method includes measuring an amount of expression of a small non-coding marker RNA in a biological sample from the patient. The method further includes comparing the measured amount of expression of the small non-coding marker RNA in the patient to a reference amount of expression of the small non-coding marker RNA.
In one embodiment, the small non-coding marker RNA is selected from SEQ ID NOs: 1-9, or variants thereof, wherein an increase of expression of the small non-coding marker RNA that is equivalent to at least 1-fold as compared to the reference amount of expression of the small non-coding marker RNA indicates an increased risk of rejection of the transplanted organ.
In another embodiment, the small non-coding marker RNA is selected from SEQ ID NOs: 10-49, or variants thereof, wherein an increase of expression of the small non-coding marker RNA that is equivalent to less than 1-fold as compared to said reference amount of expression of the small non-coding marker RNA indicates an increased risk of rejection of said transplanted organ.
In a further embodiment, the method further includes (c) measuring a difference between the amount of expression of the small non-coding marker RNA in the biological sample and the reference amount of expression of said small non-coding marker RNA; (d) measuring an amount of expression of a endogenously expressed small non-coding reference RNA in a biological sample from the patient; (e) measuring a difference between the amount of expression of the endogenously expressed small non-coding reference RNA in the biological sample from the patient and a reference amount of expression of said endogenously expressed small non-coding reference RNA; (f) comparing the difference in step (c) to the difference in step (e); wherein a difference in step (c) that is greater than the difference in step (d) further indicates an increased risk of rejection of said transplanted organ.
In yet another embodiment, the method for assessing risk of organ rejection in a patient having a transplanted organ includes: (a) measuring an amount of expression of a small non-coding marker RNA in a biological sample from the patient, said small non-coding RNA selected from SEQ ID NOs: 1-9 or a combination thereof; (b) measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the patient; (c) comparing the measured amount of step (a) to the measured amount of step (b) to determine a first ratio; (d) measuring an amount of expression of said small non-coding marker RNA in a biological sample from a person having a non-rejected organ, said small non-coding RNA selected from SEQ ID NOs: 1-9 or a combination thereof; (e) measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the person having a non-rejected organ; and comparing the measured amount of step (d) to the measured amount of step (e) to determine a second ratio; wherein a calculation of the first ratio being greater than the second ratio by an amount equivalent to at least 1-fold indicates an increased risk of rejection of said transplanted organ.
In yet a further embodiment, the method for assessing risk of organ rejection in a patient having a transplanted organ includes: (a) measuring an amount of expression of a small non-coding marker RNA in a biological sample from the patient, said small non-coding RNA selected from SEQ ID NOs: 10-49, or a combination thereof; (b) measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the patient; (c) comparing the measured amount of step (a) to the measured amount of step (b) to determine a first ratio; (d) measuring an amount of expression of said small non-coding marker RNA in a biological sample from a person having a non-rejected organ, said small non-coding RNA selected from the group consisting of SEQ ID NOs: 10-49, or a combination thereof; (e) measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the person having a non-rejected organ; and comparing the measured amount of step (d) to the measured amount of step (e) to determine a second ratio; wherein a calculation of the first ratio being greater than the second ratio by at least an amount equivalent to less than 1-fold indicates an increased risk of rejection of said transplanted organ.
In yet an additional aspect, the invention relates to a kit for assessing risk of organ rejection in a patient having a transplanted organ. The kit includes at least one nucleic acid molecule complementary to a small non-coding marker RNA selected from the group consisting of SEQ ID NO: 1-49s, or variations thereof, and a means for measuring expression of a small non-coding marker RNA in a biological sample.
The invention relates to methods and compositions for the non-invasive detection of organ rejection using a microRNA. The inventor discovered, among other things, that certain marker microRNAs (miRNA) are overexpressed or underexpressed in response to organ failure (e.g., acute rejection).
In one aspect, the invention relates to a method for assessing risk of organ rejection in a patient having a transplanted organ.
The patient having a transplanted organ is any human having a transplanted organ for which risk of organ rejection is to be assessed.
As used herein, the transplanted organ refers to any organ. Exemplary organs include kidney, heart, liver, lung, intestines, pancreas, pancreatic islets, etc.
Organ rejection refers to any failure of a transplanted organ resulting from an adverse immune response. For example, organ rejection includes acute and/or chronic rejection. An episode of acute rejection of an organ can be caused by an antibody-mediated or cell-mediated immune response. The cells involved in a cell-mediated immune response include, for example, activated cytotoxic T cells. An episode of acute rejection typcially occurs within fourteen days, more typically within ten days, and even more typically within five days after a transplant if the patient is not taking an immunosuppressant drug.
However, most if not all transplant patients are given immunosuppressant drugs. Thus, an episode of acute rejection generally occurs within about one year of a transplanted organ, more specifically within about nine months, even more specifically within about six months, and most specifically within about three months after transplant of an organ. Acute rejection, however, can occur at any time during the life of a transplanted organ. Further, a patient can have more than one episode of acute rejection of a transplanted organ.
Measuring an Amount of Expression of a Small Non-Coding Marker RNA
The method includes measuring an amount of expression of a small non-coding marker RNA in a biological sample from the patient.
As used herein, a small non-coding RNA refers to a ribonucleic acid sequence that does not code for a protein. For example, the small non-coding RNA may perform a regulatory function in the cell by regulating gene expression through sequence-specific base-pairing with complementary mRNA sequences.
A small non-coding RNA is less than about 40 nucleotides in length, preferably less than about 30 nucleotides, for example, about 29, 28, 27, 26, 25, 24, 23, 22, 21, or 20 nucleotides in length. The small non-coding RNA is more than about 10 nucleotides, for example, 11, 12, 13, 14, 15, 16, 17, 18, 19, or 20 nucleotides in length. Any maximum value can be combined with any minimum value to define a range.
Examples of a small non-coding RNA include transfer RNA (tRNA), ribosomal RNA (rRNA), microRNA (miRNA), small nuclear RNA (snRNA), small nucleolar RNA (snoRNA), and/or signal recognition particle RNA complex (SRP). Preferably, the small non-coding RNA is miRNA.
A small non-coding marker RNA as used herein refers to a small non-coding RNA that is used to assess risk of organ rejection. Specific examples of a small non-coding marker RNA include the following nucleic acid molecules and/or a nucleic acid molecule that has at least about 85%, 86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, or 99% sequence identity to a sequence set forth below:
Methods of determining sequence identity are known in the art. Percent nucleic acid sequence identity with respect to the small non-coding RNAs identified herein is defined as the percentage of nucleic acids in a candidate sequence that are identical with the nucleic acids in the specific small non-coding RNA sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity.
Alignment for purposes of determining percent nucleic acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
For purposes herein, however, percent (%) nucleic acid sequence identity values are generated using the sequence comparison computer program NCBI-BLAST2 (Altschul et al., Nucleic Acids Res. 25:3389-3402 (1997)). The NCBI-BLAST2 sequence comparison program may be downloaded from the National Center for Biotechnology Information's website or otherwise obtained from the National Institutes of Health, Bethesda, Md. NCBI-BLAST2 uses several search parameters, wherein all of those search parameters are set to default values including, for example, unmask=yes, strand=all, expected occurrences=10, minimum low complexity length=15/5, multi-pass e-value=0.01, constant for multi-pass=25, dropoff for final gapped alignment=25.
The method of the invention may include measuring an amount of expression of one small non-coding RNA or a combination of the small non-coding RNAs described above.
The small non-coding RNA is typically found in a biological sample from the patient. As used herein, a biological sample refers to any sample obtained from a patient. Exemplary biological samples include blood, urine, a tissue sample from any organ, and/or tissue sample from the transplanted organ. Urine samples are preferred.
Reference Amount of Expression of the Small Non-Coding Marker RNA
The method further includes comparing the measured amount of expression of the small non-coding marker RNA in the biological sample from the patient to a reference amount of expression of the small non-coding marker RNA.
In one embodiment, the reference amount of expression of the small non-coding marker RNA may be obtained by measuring an amount of expression of the small non-coding RNA in a person having a non-rejected organ. For example, the person having a non-rejected organ includes a healthy person. Preferably, the healthy person is a person of similar age, gender, race, graft-donor source, Banff histologic grade, and/or underwent the same initial anti-rejection treatment as the patient having a transplanted organ for which risk of organ failure is to assessed.
Another example of a person having a non-rejected organ is a person having a well-functioning (e.g., stable) transplanted organ. A well-functioning (e.g., stable) transplanted organ may be defined as a transplanted organ that does not exhibit organ failure (e.g., rejection). Preferably, a well-functioning transplanted organ is a transplanted organ that has not developed transplant dysfunction or morphologic evidence of transplant injury in areas of the transplant. For example, a stable functioning kidney transplant may be defined as having a serum creatinine concentration that has not changed by more than approximately 0.2 mg per deciliter during the seven days before and the seven days after collection of the biologic specimen for measurements of the small non-coding RNA. Preferably, the person having a well-functioning (e.g., stable) transplanted organ is a person of similar age, gender, race, graft-donor source, Banff histologic grade, and/or underwent the same initial anti-rejection treatment as the patient having a transplanted organ for which risk of organ failure is to assessed.
In another embodiment, the reference amount is obtained by measuring an amount of expression of said small non-coding RNA in a second biological sample from the patient. For example, the second biological sample may be obtained from the patient before the organ transplantation and/or from another non-rejected organ of the patient.
In yet another embodiment, the reference amount of expression of the small non-coding RNA is a value for expression of the small non-coding RNA that is accepted in the art.
Comparing the Measured Amount of Expression of the Small Non-Coding Marker RNA
The method includes comparing the measured amount of expression of the small non-coding RNA to the reference amount of expression of the small non-coding RNA. The small non-coding marker RNA may be, for example, a small non-coding RNA selected from SEQ ID NOs: 1-53, or variants thereof. Preferably the small non-coding marker RNA is selected from SEQ ID NOs 1: 49, or variants thereof.
In a more preferred embodiment, the small non-coding marker RNA is selected from a sequence set forth in SEQ ID NOs: 1-9, or a variation thereof. For example, the small non-coding marker RNA includes a small non-coding RNA selected from miR-142-5p; miR-142-3p; miR-155; miR-223; miR-146a; miR-146b; miR-342; miR-650; miR-21; and/or miR-425-5p, or a combination thereof, wherein an increase of expression of the small non-coding marker RNA that is equivalent to at least about 1-fold as compared to the reference amount of expression of the small non-coding marker RNA indicates an increased risk of rejection of the transplanted organ. In a most preferred embodiment, the small non-coding marker RNA is miR-142-5p; miR-142-3p; and/or miR-155.
An increase of expression that is equivalent to at least about 1-fold may be an increase in an amount equivalent to at least about 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-fold, or more as compared to the increase in the reference amount of expression of the small non-coding marker RNA. Preferably, the increase is a fold value. Examples of methods to quantify an increase of expression are known in the art, as are described in the General Methods section below.
An increased risk of organ rejection varies in different patients and the type of organ transplanted. Generally, the increased risk is at least about 25%, at least about 50%, at least about 75%, or at least about 90% as compared to a person having no risk of organ rejection.
Conversely, in one embodiment, an increase of expression of the small non-coding marker RNA selected from a sequence set forth in SEQ ID NOs: 1-9, or a variation thereof, that is equivalent to about less than 1-fold, as compared to the reference amount of expression of the small non-coding marker RNA, indicates a decreased risk of rejection of the transplanted organ. The decreased risk of organ rejection varies in different patients and the type of organ transplanted. Generally, the decreased risk is at least about 25%, at least about 50%, at least about 75%, or at least about 90% as compared to a person having no risk of organ rejection.
In another preferred embodiment, the small non-coding marker RNA is selected from a sequence set forth in SEQ ID NOs: 10-49, or a variation thereof. For example, the small non-coding marker RNA includes a small non-coding RNA selected from miR-30c; miR-30a-3p; miR-10a; miR-30e-3p; miR-30b; miR-10b; miR-32; miR-9; miR-193b; miR-143; miR-489; miR-27b; miR-126; miR-378; miR-429; miR-181c; miR-196b; miR-199a; miR-660; miR-203; miR-204; miR-30e-5p; miR-30a-5p; miR-30d; miR-125b; miR-130a; miR-126; miR-195; miR-26a; miR-26b; miR-497; miR-152; miR-141; miR-296; miR-365; miR-99a; miR-100; miR-186; and/or let-7a, wherein an increase of expression of the small non-coding RNA that is equivalent to less than 1-fold as compared to the reference amount of expression of the small non-coding marker RNA indicates an increased risk of rejection of the transplanted organ.
An increase of expression that is equivalent to less than 1-fold may be an increase of at most about 0.9-, 0.8-, 0.7-, 0.6-, 0.5-, 0.4-, 0.3-, 0.2-, or 0.1-fold, or less as compared to the increase in the reference amount of expression of the small non-coding marker RNA. Preferably, the increase is a fold value. Examples of methods to quantify an increase of expression are known in the art, as are described in the General Methods section below.
Conversely, in one embodiment, an increase of expression of the small non-coding marker RNA selected from a sequence set forth in SEQ ID NOs: 10-49, or a variation thereof, equivalent to at least about 1-fold, or more, as compared to the reference amount of expression of the small non-coding marker RNA, indicates a decreased risk of rejection of the transplanted organ. The decreased risk of organ rejection varies in different patients and the type of organ transplanted. Generally, the decreased risk is at least about 25%, at least about 50%, at least about 75%, or at least about 90% as compared to a person having no risk of organ rejection.
Use of an Endogenously Expressed Small Non-Coding Reference RNA to Further Indicate an Increased Risk of Organ Rejection
Measuring and Comparing an Amount of an Endogenously Expressed Small Non-Coding Reference RNA
In yet another embodiment, the method for assessing risk of organ rejection further includes measuring an amount of an endogenously expressed small non-coding reference RNA in a biological sample from the patient. In addition, the method includes measuring a reference amount of an endogenously expressed small non-coding reference RNA in a biological sample.
The reference amount may be obtained by measuring the amount of expression of the endogenously expressed small non-coding reference RNA in a person having a non-rejected organ or in a second biological sample from the patient, as described above. In another embodiment, the reference amount is a value for expression of the endogenously expressed small non-coding reference RNA that is accepted in the art.
An endogenously expressed small non-coding reference RNA refers to a small non-coding RNA that is endogenously expressed (e.g., expressed within the patient, cell, and/or tissue) and demonstrates an expression that is relatively constant and abundant in the biological sample.
Methods of selecting and validating the endogenously expressed small non-coding reference RNA are known in the art. See, for example, TaqMan® MicroRNA Assays from Applied Biosystems. Preferably, the endogenously expressed small non-coding reference RNA is stable, has a similar size as the measured small non-coding RNA (e.g., SEQ ID NOs: 1-53), and is amenable to means for measuring expression.
Examples of endogenously expressed small non-coding reference RNA include RNU24, RNU66, RNU19, RNU38B, RNU49, Z30, RNU6B, RNU48, RNU43, and/or RNU44. Preferably, the endogenously expressed small non-coding reference RNA is endogenous small nucleolar RNA RNU44.
Measuring a Difference in Expression of Marker RNA to Reference RNA
In a preferred embodiment, the method further includes measuring a difference between the amount of expression of the small non-coding marker RNA in the biological sample and the reference amount of expression of the small non-coding marker RNA. For example, the method can include measuring the difference between the amount of expression of the small non-coding marker RNA in the biological sample from the patient and the reference amount of expression of the small non-coding marker RNA.
As explained above, the reference amount may be obtained by measuring the amount of expression of the endogenously expressed small non-coding reference RNA in a person having a non-rejected organ or in a second biological sample from the patient, as described above. In another embodiment, the reference amount is a value for expression of the endogenously expressed small non-coding reference RNA that is accepted in the art.
The embodiment further includes measuring a difference between the amount of expression of the endogenously expressed small non-coding reference RNA in the biological sample and the reference amount of expression of the endogenously expressed small non-coding reference RNA. Or example, the method includes measuring the difference between the amount of expression of the endogenously expressed small non-coding reference RNA in the biological sample from the patient and the reference amount of expression of the endogenously small non-coding reference RNA.
As explained above, the reference amount may be obtained by measuring the amount of expression of the endogenously expressed small non-coding reference RNA in a person having a non-rejected organ or in a second biological sample from the patient, as described above. In another embodiment, the reference amount is a value for expression of the endogenously expressed small non-coding reference RNA that is accepted in the art.
The embodiment further includes comparing (i) the difference in amount of expression of the small non-coding marker RNA between the patient sample and the reference amount and (ii) the difference in amount of expression of the endogenously expressed small non-coding reference RNA between the patient sample and the reference amount. When the difference in (i) (i.e., expression of the small non-coding marker RNA between the patient sample and the reference amount) is greater than the difference in (ii) (i.e., the amount of expression of the endogenously expressed small non-coding reference RNA between the patient sample and the reference amount), the comparison further indicates an increased risk of rejection of the transplanted organ.
Preferably, a difference in (i) that is greater than the difference in (ii) by an amount equivalent to at least about 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-fold, or more, indicates an increased risk of rejection of the transplanted organ.
In another preferred embodiment, a difference in (i) that is greater than the difference in (ii) by an amount equivalent to less than 1-fold, for example, at most about 0.9-, 0.8-, 0.7-, 0.6-, 0.5-, 0.4-, 0.3-, 0.2-, or 0.1-fold, or less, indicates an increased risk of rejection of the transplanted organ.
Accordingly, the present embodiment relates to one example by which one skilled in the art may measure and/or determine whether the increase in expression of the small non-coding RNA, as compared to the reference amount, is statistically significant in the patient.
Normalizing
In a preferred embodiment, the invention includes normalizing the amount of expression of the small non-coding marker RNA. The method includes measuring an amount of expression of a small non-coding marker RNA in a biological sample from the patient, as described above. The method further includes measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the patient. In addition, the method includes comparing the measured amount of the small non-coding marker RNA from the patient to the measured amount of endogenously expressed small non-coding reference RNA from the patient to determine a first ratio.
The method further includes measuring an amount of expression of the small non-coding marker RNA in a biological sample from a person having a non-rejected organ. The method further includes measuring an amount of expression of an endogenously expressed small non-coding reference RNA in a biological sample from the person having a non-rejected organ. In addition, the method includes comparing the measured amount of the small non-coding marker RNA from the person having a non-rejected organ to the measured amount of endogenously expressed small non-coding reference RNA from the person having a non-rejected organ to determine a second ratio.
When a calculation of the first ratio is greater than the second ratio by an amount equivalent to at least 1-fold, the calculation indicates an increased risk of rejection of said transplanted organ in the patient having a transplanted organ. The calculated increase of the first ratio over the second ratio that is at least 1-fold may be an increase that is equivalent to at least about 1-, 2-, 3-, 4-, 5-, 6-, 7-, 8-, 9-, 10-, 11-, 12-, 13-, 14-, 15-, 16-, 17-, 18-, 19-, 20-fold, or more.
When a calculation of the first ratio is greater than the second ratio by an amount equivalent to less than 1-fold, the calculation indicates an increased risk of rejection of said transplanted organ in the patient having a transplanted organ. The calculated increase of the first ratio over the second ratio may be an increase that is equivalent to less than 1-fold may be an increase of at most about 0.9-, 0.8-, 0.7-, 0.6-, 0.5-, 0.4-, 0.3-, 0.2-, or 0.1-fold, or less.
Accordingly, in the present embodiment, fold changes or equivalents thereof for the small non-coding marker RNA are normalized to the endogenously expressed small non-coding reference RNA.
Serum Creatinine and Additional Embodiments
In one embodiment, when the transplanted organ is a kidney, the method for assessing risk of organ rejection in a patient may further include determining the amount of serum creatinine protein in the patient. The determination of the amount of serum creatinine can be made by any method known to those skilled in the art, such as those described in U.S. Patent Publication US20080131441, which is incorporated by reference herein.
In this embodiment, the measured amount of serum creatinine in the patient is compared to a control amount of serum creatinine of a healthy person or a person having a well-functioning (e.g., stable) transplant, as described in U.S. Patent Publication 20080131441, which is incorporated by reference herein. For example, the normal level of serum creatinine in a healthy person or a person with a well-functioning transplant is generally about 0.8-1.6 milligrams/deciliter. The person may be the patient or a person different from the patient.
It is not necessary to determine the level of creatinine in a control sample every time the method is conducted. For example, the serum creatinine level from the patient can be compared to that of one or more previously determined control samples or to a level recognized by the physician or clinician conducting the method, or by a consensus of medical and/or clinical practitioners.
In another embodiment, the method further includes informing the patient whether the patient is at decreased or increased risk of organ rejection. The information that a patient is at risk of rejection of a transplanted organ is useful. Such patients can be prescribed and/or administered a treatment to prevent rejection and/or loss of the transplanted organ.
In one embodiment, the treatment includes administering to the patient an effective amount of a pharmaceutical composition to prevent rejection and/or loss of the transplanted organ. Such pharmaceutical compositions are well known to those skilled in the art, and include, for example a steroid pulse, an antibody, etc.
For example, a steroid pulse therapy can include the administration for three to six days of a high dose corticosteroid (e.g., greater than 100 mg). An example of an antibody therapy includes the administration for seven to fourteen days of the polyclonal antibody Thymoglobin or the monoclonal antibody, OKT3.
Another example of a treatment that can be administered is plasmapheresis. Plasmapheresis is a process in which the fluid part of the blood (i.e., plasma) is removed from blood cells. Typically, the plasma is removed by a device known as a cell separator. The cells are generally returned to the person undergoing treatment, while the plasma, which contains antibodies, is discarded.
Each of the methods and embodiments of the present invention can be used alone, or in combination with one or more, or all, of the other methods.
General Methods
A biological sample from a patient or person can be obtained by any method known to those in the art. In addition to the examples described above, further examples of biological samples include transplant tissue biopsy, blood, urine, bile, bronchioalveolar lavage fluid, and pericardial fluid. Suitable methods include, for example, venous puncture of a vein to obtain a blood sample, collection of a urine specimen, and a percutaneous core needle biopsy.
Any method known to those in the art can be employed for determining the amount of a small non-coding RNA. Typically, total RNA is isolated from the biological sample. RNA can be isolated from the sample by any method known to those in the art. For example, commercial kits, such as the TRI Reagent® commercially available from Molecular Research Center, Inc. (Cincinnati, Ohio), or the mirVana miRNA isolation kit from Ambion, can be used to isolate RNA. The yield and purity of RNA can be measured using a NanoDrop ND-1000 spectrophotometer.
The quantification of small non-coding RNA from total mRNA from the biological sample can be performed by any method known to those in the art. For example, kinetic, quantitative PCR involves reverse transcribing the total RNA (e.g., by using the Taqman Multiplex RT set for TaqMan Array Human MicroRNA Panel v1.0) and polymerase chain reaction (PCR). Quantitative PCR can be carried out on an Applied BioSystems 7900HT thermocycler, or an equivalent thereof, using the manufacturer's recommended cycling conditions. Briefly, cDNA can be reverse transcribed from the total RNA samples using specific small non-coding RNA primers, which may be obtained from the TaqMan MicroRNA assays (Applied Biosystems) and reagents from the TaqMan microRNA reverse transcription kit (Applied Biosystems).
Generally, the isolated small non-coding RNA may be amplified by methods known in the art. Amplification systems utilizing, for example, PCR or RT-PCR methodologies are known to those skilled in the art. For a general overview of amplification technology, see, for example, Dieffenbach et al., PCR Primer: A Laboratory Manual, Cold Spring Harbor Laboratory Press, New York (1995). For example, the amounts of small non-coding RNA can be determined using kinetic, quantitative PCR. Preferably, PCR products are amplified from cDNA samples using the TaqMan microRNA assay (Applied Biosystems).
An alternative method for determining the amount of small non-coding RNA expression includes the use of molecular beacons and other labeled probes useful in, for example multiplex PCR. In a multiplex PCR assay, the PCR mixture contains primers and probes directed to the small non-coding RNA PCR product. Typically, a single fluorochrome is used in the assay. The molecular beacon or probe is detected to determine the amount of small non-coding RNA. Molecular beacons are described, for example, by Tyagi and Kramer (Nature Biotechnology 14, 303-308, 1996) and by Andrus and Nichols in U.S. Patent Application Publication No. 20040053284.
Another method includes, for instance, quantifying cDNA (obtained by reverse transcribing the small non-coding RNA) using a fluorescence based real-time detection method, such as the ABI PRISM 7700 or 7900 Sequence Detection System [TaqMan®)] commercially available from Applied Biosystems, Foster City, Calif. or similar system as described by Heid et al., (Genome Res. 1996; 6:986-994) and Gibson et al. (Genome Res. 1996; 6:995-1001).
Small non-coding marker RNA copy numbers can then be normalized using an endogenously expressed small non-coding reference RNA copy number and the abundance of the small non-coding marker RNA can be expressed as a ratio of the small non-coding marker RNA to the endogenously expressed small non-coding reference RNA.
Generally, the amount of small non-coding RNA expression in a biological sample is significantly greater if the expression of small non-coding RNA is heightened. For example, a discriminatory level for heightened gene expression (e.g., the baseline magnitude of expression) of the small non-coding RNA is defined as the mean±95% confidence interval of a group of values observed in non-rejecting organs (e.g., control values, i.e., control levels). The group of values as used herein includes, for example, a minimum of at least about 2 values, more preferably a minimum of at least about 10 values, most preferably a minimum of at least about 20 values. The group of values as used herein includes, for example, a maximum of at most about 500 values, more preferably a maximum of at most about 100 values, most preferably a maximum of at most about 50 values.
Heightened expression of the small non-coding RNA is considered to be significantly greater if the value is greater than the mean±95% confidence interval of a group of values observed in non-rejecting organs. Similarly, the level of the small non-coding RNA in the cell sample is considered to be significantly lower if the amount of expression of the small non-coding RNA is lower than the mean±95% confidence interval of a group of values observed in non-rejecting organs.
The amount of expression of the small non-coding RNA is typically considered not significantly greater if the level of the small non-coding RNA in the biological sample is not greater than the mean±95% confidence interval of a group of values observed in non-rejecting organs. The amount of expression of the small non-coding RNA is normally considered not significantly lower if the amount in a biological sample is not lower than the mean±95% confidence interval of a group of values observed in nonrejecting transplants.
Statistical analysis in the above mean±95% confidence interval of a group of values observed in non-rejecting organs may be performed with a x2 test.
In another embodiment, the amount of expression of the small non-coding marker RNA in a biological sample is significantly greater if the log-transformed mean (±SE) ratio of the small non-coding marker RNA copies to the endogenously expressed small non-coding reference RNA copies is higher relative to a control ratio in non-rejecting organs, as determined by the Kruskal-Wallis test. For example, a significantly greater ratio is typically at least about ±SE 3.0, more typically between ±SE 3.0 and 5.0, and most typically between ±SE 3.8 and 4.7.
Similarly, the amount of the small non-coding RNA in a biological sample is significantly lower if the log-transformed mean (±SE) ratio of the small non-coding marker RNA copies to the endogenously expressed small non-coding reference RNA copies is reduced relative to a control ratio (i.e., control values, control levels) in non-rejecting organs, as determined by the Kruskal-Wallis test. For example, a typical non-rejecting organ control ratio is not more than about 2.5, more typically 1.0 to 2.5, and most typically from 1.3 and 2.0.
In an embodiment of the invention, generally, the amount of small non-coding RNA when compared to a control amount may be increased by at least about 10%, at least about 50%, or at least about 100%. The amount of expression level of a small non-coding RNA when compared to a control amount may be decreased by at least about 10%, at least about 50%, or at least about 100% lower.
It is not necessary to determine the amount of expression of the small non-coding marker RNA or the endogenously expressed small non-coding reference RNA in a every time the method is conducted. For example, the amount of small non-coding marker or reference RNA in the biological sample from the transplanted organ can be compared to that of one or more previously determined control samples or compared to an amount recognized by the physician or clinician conducting the method of a consensus of medical and/or clinical practitioners.
With respect to serum creatinine, any method known in the art can be used for determining the amount of serum creatinine in the biological sample. Suitable methods for determining protein levels include an ELISA and a standard blot. Briefly, these assays are normally based on incubating an antibody specific to the protein with a sample suspected of containing the protein, and detecting the presence of a complex between the antibody and the protein.
Alternatively, commercial kits can be utilized. An example of a commercial kit for determining creatinine level is the QuantiChrom™ Creatinine Assay Kit from BioAssay Systems (Hayward, Ca).
Kit
In another aspect, the invention relates to a kit for assessing risk of organ rejection in a patient having a transplanted organ. The kit includes at least one nucleic acid molecule complementary to a small non-coding marker RNA selected from SEQ ID NOs: 1-49, or variations thereof. The kit further includes a means for measuring expression of a small non-coding marker RNA in a biological sample. The kit may also include written instructions for a method of assessing risk of organ rejection, as described above.
In a preferred embodiment, the means for measuring expression includes quantitative polymerase chain reaction. Additional means for measuring expression include those described under General Methods.
MicroRNA Expression Profiles of Human Renal Allografts. We first determined global miRNA expression profiles of human renal allografts using microfluidic cards containing TaqMan primers and probes for 365 mature human miRNAs. The characteristics of patients whose renal allograft biopsies were studied for global miRNA expression patterns (training set), or for a subset of differentially expressed miRNAs (validation set), are summarized in Table 1.
Among the 365 mature human miRNAs analyzed in the training set (4 normal and 3 AR biopsies), 174±7 miRNAs (48%) were expressed in each biopsy sample (174±10 miRNAs in the AR biopsies vs. 174±4 miRNAs in the normal allograft biopsies). Unsupervised hierarchical clustering of miRNA expression patterns correctly classified the normal allograft biopsies and the AR biopsies (
The clear separation of AR biopsies from normal allograft biopsies was further confirmed by displaying the relationships among miRNA expression patterns using principal component analysis (PCA) (
MicroRNAs Distinguishing Acute Rejection Biopsies from Normal Allograft Biopsies. Supervised analysis was used to detect miRNAs differentially expressed in AR biopsies and normal allograft biopsies. A subset of 17 miRNAs was differentially expressed at a P value<0.01. Among the 17 miRNAs, 10 (let-7c, miR-10a, miR-10b, miR-125a, miR-200a, miR-30a-3p, miR-30b, miR-30c, miR30e-3p, and miR-32) were underexpressed in AR biopsies compared to normal allograft biopsies, and 7 (miR-142-5p, miR-142-3p, miR-155, miR-223, miR-146b, miR-146a, and miR-342) were overexpressed (
‡Two sequences corresponding to miR-126 have been quantified in the microfluidic cards.
Validation of the MicroRNA Signatures Predictive of Renal Allograft Status. An independent set of 26 renal allograft biopsies (9 AR biopsies and 17 normal allograft biopsies) was used to validate a subset of miRNAs identified by global expression profiling to be differentially expressed in AR biopsies and normal allograft biopsies.
Intragraft mirRNA Levels Are Biomarkers of Renal Allograft Status. We investigated whether intragraft miRNA levels predict AR and renal allograft function. We used receiver-operating curves (ROCS) to analyze miRNA levels to determine cutoff points that yielded the highest combined sensitivity and specificity for predicting AR and allograft function. Our analysis showed that AR can be predicted very accurately using intragraft levels of miR-142-5p (100% sensitivity and 95% specificity, P<0.0001, Table 1) or miR-155 (100% sensitivity and 95% specificity, P<0.0001, Table 1). Intragraft levels of miR-223, -10b, -30a-3p, and let-7c were also diagnostic of AR but with a lesser level of accuracy (Table 1).
Analysis involving the ROC showed that AR can also be predicted using intragraft levels of T cell CD3 mRNA, B cell CD20 mRNA, and mRNA encoding renal tubular proteins NKCC-2 and USAG-1 but with much less sensitivity and specificity compared to intragraft levels of miR-142-5p, -155, or -223 (Table 1).
We examined whether intragraft miRNA levels predict renal allograft function. Renal graft function at the time of allograft biopsy was assessed by calculating glomerular filtration rate (eGFR) using the 4-parameter modified diet in renal disease (MDRD) formula. Our examination showed that intragraft levels of miR-142-5p (R=−0.66, P<0.0001), -10b (R=0.62, P<0.0001), -155 (R=−0.59, P=0.0003), -223 (R=−0.57, P=0.0006), -30a-3p (R=0.57, P=0.0006), and let-7c (R=0.37, P=0.03) are significantly associated with eGFR. Among the intragraft mRNAs assessed, CD3 mRNA (R2=0.36, P=0.0002), but not mRNA for CD20 (R2=0.04, P=0.25), NKCC-2 (R2=0.01, P=0.58), or USAG-1 (R2=0.08, P=0.21), was associated with graft function.
Mechanisms for the Altered Intragraft Expression of miRNAs in AR Biopsies.
We examined whether an association exists between miRNAs underexpressed in AR biopsies and intragraft mRNA levels. We found a positive association between renal tubule-specific NKCC-2 mRNA and miR-30a-3p (
To address whether the altered expression of miRNAs in AR biopsies is because of the relative proportions of graft-infiltrating immune cells and resident kidney parenchymal cells, we quantified the abundance of differentially expressed miRNAs in normal human PBMCs and in normal HRECs. We also investigated whether stimulation of PBMCs or HRECs altered the level of expression of miRNAs. Our investigation showed that whereas the absolute levels of RNU44 small nucleolar miRNA was similar in both PBMCs and HRECs (2.0×107±1.2×107 vs. 2.35×107+1.9×106, P>0.05), the miRNAs overexpressed in AR biopsies (miR-142-5p, miR-155, and miR-223) were all expressed at a higher level in normal human PBMCs compared to miRNAs (miR-30a-3p, miR-10b, or let-7c) underexpressed in AR biopsies. Moreover, stimulation of PBMCs with the mitogen phytohaemagglutinin (PHA) results in an increase in the abundance of miR-155 (P=0.0002) and a decrease in miR-223 (P=0.02), let-7c (P=0.02), or miR-142-5p (P=0.08) (
Quantification of miRNAs in primary cultures of HRECs showed that miR-30a-3p, miR-10b, or let-7c are expressed at a higher level in HRECs compared to PBMCs, and that stimulation of HRECs with cell-free supernatants of PHA-activated PBMCs results in a decrease in the abundance of miR-30a-3p (P=0.02) (
We investigated microRNA expression patterns of 33 renal allograft biopsies obtained from 32 adult recipients of human renal allografts: 12 biopsies from 11 recipients with graft dysfunction [mean (±SD) creatinine: 5.6±3.5 mg/dL] and biopsy-confirmed AR according to the Banff 97 classification [mean age (±SD): 38.5±8.6 yr, 7 men and 4 women, 5 living and 6 deceased donors] and 21 biopsies from 21 recipients with stable allograft function (creatinine: 1.3±0.3 mg/dL) and normal allograft biopsy (46.4±11.5 yr, 8 men and 13 women, 15 living and 6 deceased donors). The mean (±SE) time to biopsy was 19.1±7.0 months posttransplantation in the AR group and 6.3±0.9 months in the group with stable graft function and normal biopsy results (P=0.51, Maim-Whitney test). Additional information of the study subjects is given in Table 1 and in the discussion below.
MicroRNA Expression Profiling. Global miRNA profiling of allograft biopsy specimens was studied using the TaqMan low-density array human microRNA panel v1.0 containing 365 mature human miRNAs (Applied Biosystems). miRNAs found to be differentially expressed in AR biopsies compared to normal allograft biopsies were quantified using TaqMan miRNA assays (Applied Biosystems) modified by the incorporation of our standard curve protocol. Details for total RNA purification, miRNA profiling, quantification, and data analysis are provided below.
The expression level of mRNAs was quantified using real-time quantitative PCR assays as detailed below. Primers and probes sequences are shown in Table 4, below.
Cell Culture. The procedures for the in vitro studies using peripheral blood mononuclear cells and normal human renal epithelial cells are described below.
Human Renal Allograft Biopsy Classification. Percutaneous core needle biopsies were obtained and formalin-fixed, paraffin embedded renal biopsies were stained with hematoxylin and eosin, periodic acid-Schiff and Masson's trichrome, and analyzed by a pathologist, blinded to the results of molecular studies using the Banff 97 classification. Immunosuppression consisted of a calcineurin inhibitor-based regimen, with methyl prednisolone for the initial treatment of acute rejection. The study was approved by the Institutional Review Board at the Weill Cornell Medical College, and each patient gave written informed consent.
Global MicroRNA Expression Profiling. Allograft biopsy samples were placed in RNAlater (Ambion) and stored at −80° C. until RNA extraction. Total RNA was extracted from biopsies using the mirVana miRNA isolation kit according to the manufacturer's specification (Ambion). The yield and purity of RNA were measured using a NanoDrop ND-1000 spectrophotometer (Nanodrop Technologies), and RNA integrity was assessed using the RNA 6000 Nano LabChip kit (Agilent Technologies). We used the TaqMan Low-Density Array Human MicroRNA Panel v1.0 (Applied Biosystems), a 384-well microfluidic card that contains primers and probes for 365 different human miRNAs in addition to 2 small nucleolar RNAs that function as endogenous controls for data normalization, for global miRNA profiling of allograft biopsy specimens. Three acute rejection (AR) biopsy samples and 4 normal kidney allograft biopsy specimens were profiled for global miRNA gene expression patterns (7 biopsies, training set). Total RNA (480 ng) was reverse transcribed using the TaqMan Multiplex RT set for TaqMan Array Human MicroRNA Panel v1.0. Each RT reaction was diluted 62.5-fold with water, and 55 μL of each diluted product was combined with 55 μL of TaqMan 2× Universal PCR Master Mix, No AmpErase UNG. One-hundred microliters of the sample/master mix for each Multiplex pool were loaded into fill reservoirs of the microfluidic card; the array was then centrifuged and mechanically sealed with the Applied Biosystems sealer device. Quantitative PCR was carried out on an Applied BioSystems 7900HT thermocycler using the manufacturer's recommended cycling conditions. Fold changes for each miRNA were normalized to the endogenous control RNU44 small nucleolar RNA. The relative expression levels between samples were calculated using the comparative delta CT (threshold cycle number) method with a control sample (normal) as the reference point.
TaqMan Low-Density Array Analysis. Data analysis was performed by using the SDS software version 2.3 and the baseline and threshold were automatically set. Data were normalized and then analyzed to define genes that are differentially expressed between the AR biopsies and normal protocol biopsies. Assays that had CT values>35 were removed from the analysis. The delta CT values were calculated by using RNU44 as the endogenous control. Unsupervised clustering method and principal component analysis (PCA) were used to visualize patterns in the data set without any a priori sample classification. Average linkage clustering analysis was implemented in the Cluster program and Java Tree View 1.0 .12 software. PCA were done using the xlstat software. Data were analyzed using Applied Biosystem's ABqPCR data analysis tool (Applied Biosystems, personal communication). A Student t test was performed to detect differentially expressed miRNAs between the AR samples and normal allograft biopsies.
Quantification of MicroRNAs. miRNAs found to be differentially expressed in AR biopsies compared to normal allograft biopsies by the TaqMan Low-Density Array were measured using Taq-Man miRNA assays (Applied Biosystems) in 9 additional AR samples and 17 additional normal allograft biopsies (26 biopsies, validation set). TaqMan miRNA assays were also used to quantify miRNA in the in vitro experiments. Reverse transcription for individual miRNAs was performed using the TaqMan microRNA reverse transcription kit (Applied Biosystems). Briefly, cDNA were reverse transcribed from total RNA samples using specific miRNA primers from the TaqMan microRNA assays (Applied Biosystems) and reagents from the TaqMan microRNA reverse transcription kit (Applied Biosystems). Each reverse transcription reaction consists of 7 μL master mix, 3 μL miRNA-specific primer, and 5 μL of 1 ng/μL dilution of total RNA. Reverse transcription was done in Veriti thermal cyclers (Applied Biosystems), using the following parameter values: 16° C. for 30 min, 42° C. for 30 min, and 85° C. for 5 min. PCR products were amplified from cDNA samples using the TaqMan microRNA assay (Applied Biosystems). PCR for each sample was set up in duplicate as a 20-μL reaction volume using 1 μL 20X TaqMan miRNA assay (Applied Biosystems) containing a mix of miRNA-specific forward PCR primer, a specific reverse PCR primer, and a miRNA-specific TaqMan MGB probe, TaqMan Universal PCR Master Mix, and 1.5 μL cDNA. A synthetic amplicon was used to develop a standard curve (see below) and TaqMan CT values were converted into absolute copy numbers. See, N Engl J Med 358:353-361. miRNA copy numbers were normalized using RNU44 small nucleolar RNA copy numbers and the abundance of miRNAs was expressed as a ratio of miRNA copies to RNU44 copies (miRNA copies in 1 μg RNA/RNU44 small nucleolar RNA copies in 1 μg RNA). TaqMan microRNA assays were performed using an ABI Prism 7500 real-time PCR system.
Quantification of Messenger RNAs. Levels of mRNAs were measured using an ABI Prism 7500 Fast detection system (Applied Biosystems). PCR for each sample was set up in duplicate as a 20-μL reaction volume using 10 μL TaqMan Universal PCR Master Mix, 2.5 μL preamplified template cDNA, 0.15 μL primers (sense primer and antisense primer, 50 μM each; Table 4 lists the oligonucleotide primers and probes), 0.05 μL probe (100 μM), and 7.34 μL of water. The PCR amplification protocol consists of an initial hold at 95° C. for 20 seconds and 40 cycles of denaturing at 95° C. for 3 seconds and primer annealing and extension at 60° C. for 30 seconds. Transcript levels are calculated using our standard curve method (see below), and mRNA copy numbers are normalized using 18S rRNA copy numbers (mRNA copies in 1 μg RNA/18S rRNA copies in 1 ng RNA).
Method for Absolute Quantification of mRNAs and miRNAs. RNA levels (mRNA and miRNA) were calculated using our previously described standard curve method, incorporated by reference herein from Kawai T, et al. (2008) HLA-mismatched renal transplantation without maintenance immunosuppression. N Engl J Med 358:353-361. The standard curve was established using PCR generated 73-bp mouse Bak amplicon as the standard. The Bak amplicon was generated in a PCR using GeneAmp 9600 thermal cycler and with 3 μL cDNA and 22 μL of dNTP, 10μ PCR buffer, TaqDNA polymerase, and Bakspecific oligonucleotide primer pair [sense primer: 5′ CCCACATCTGGAGCAGAGTCA 3′ (192-212) (SEQ ID NO:84); antisense primer: 5′ CAGATGCCATTTTTCAGGTCTTG 3′ (264-242) (SEQ ID NO:85), accession no. Y13231]. The PCR product was separated by electrophoresis with a 2% agarose gel and the amplicon size (73 bp) was confirmed using a DNA size standard of pUC mix marker 8 (Crystalgen). The Bak amplicon was isolated and purified from the gel with QIAquick gel extraction kit (QIAGEN). The absolute quantity of the purified amplicon was measured by A260 and converted to the number of copies using the molecular weight of DNA. The Bak amplicon was diluted to the concentration of 107 copies/μL (stock solution). When a standard curve was to be established for the real-time quantitative PCR assay, the stock solution was diluted over 6 orders of magnitude (1,000,000, 100,000, 10,000, 1,000, 100, and 10 copies per 1 μL) (work solution). Work solution (2.5 μL) was added to duplicate wells and amplified with Bak-specific primer pair and Bakspecific fluorogenic TaqMan probe [5′ FAM CAGGTGACAAGTGACGGTGGTCTCCA TAMRA 3′ (215-240) (SEQ ID NO:86)]. The threshold cycles (CT) were then plotted vs. the log of the initial amount of the Bak amplicon to develop the standard curve. The thresholds were in the exponential phase of the PCR and the higher the initial copy number of the Bak amplicon, the lower was the CT value.
Isolation of Normal Human Peripheral Blood Mononuclear Cells and Activation with Phytohaemagglutinin. Peripheral blood mononuclear cells (PBMCs) were obtained from whole blood of 7 healthy volunteers by standard Ficoll density-gradient centrifugation. PBMCs were resuspended at 106 cells/mL in RPMI 1640 (Gibco BRL) containing 5% (vol/vol) heat-inactivated FCS, penicillin (100 U/mL), streptomycin sulfate (100 μg/mL), and L-glutamine (4 mM). The PBMCs (106/mL) were incubated without or with phytohaemagglutinin (PHA) (Remel) at a final concentration of 2 μg/mL. Following incubation for 24, 48, or 72 h at 37° C. in 5% CO2 humidified atmosphere, the cells were retrieved, washed twice with PBS, and pelleted by centrifugation. Six hundred microliters of lysis/binding buffer from the mirVana miRNA isolation kit (Ambion) were added directly to the cell pellet. Lysates were stored at −80° C. or total RNA was immediately extracted using the manufacturer's recommended protocol for total RNA isolation. Cell-free supernatants of PBMCs incubated without or with 2 μg/mL PHA were collected by centrifugation and concentrated (Amicon, Millipore) for the in vitro studies using human renal epithelial cells.
Human Renal Epithelial Cells Culture. Normal human renal tubular epithelial cells (HRECs) were harvested from human nephrectomy specimens removed for renal cell carcinoma and isolated according to previously published methods, with minor modifications. Fragments of nontumoral renal cortex were minced and digested with collagenase IV (250 IU/mL) for 3 h at 37° C. Cells were centrifuged and the pellets washed 3 times with PBS. Cells were then cultured in Dulbecco's modified Eagle medium (DMEM) containing 5 μg/mL insulin, 10 μg/mL human apotransferrin, 500 ng/mL hydrocortisone, 10 ng/mL EGF, 6.5 ng/mL triiodothyronin, 5 ng/mL sodium selenite, 1% FCS, 25 IU/mL penicillin, 25 μg/mL streptomycin, and 10 mM Hepes buffer. HRECs were then incubated at 37° C. in 5% CO2 and 95% air. The characterization of our cellular model has been published previously, confirming the proximal descent of the vast majority of the cultured tubular epithelial cells. Experiments were not performed with HRECs beyond the third passage. HRECs were harvested at 80% confluence and seeded in 60-mm dishes at 3×105 cells/dish. At 50% confluence, cells were treated with various amounts of concentrated cell-free supernatants of PBMCs incubated without or with 2 μg/mL PHA. Following 24 or 48 h of culture at 37° C. in 5% CO2-95% air-humidified atmosphere, the HRECs were retrieved and washed twice with PBS. Six hundred microliters of lysis/binding buffer from the mirVana miRNA isolation kit (Ambion) were added directly to the culture plate to lyse the cells. Lysates were harvested manually with a sterile cell scraper and transferred to a 1.5-mL tube. Samples were stored at −80° C. or RNA was immediately extracted using the manufacturer's recommended protocol for total RNA isolation.
Statistical Analysis. We used a conventional receiver-operating characteristic (ROC) curve to analyze mRNA and miRNA levels to determine the cutoff points that yielded the highest combined sensitivity and specificity with respect to distinguishing subjects with acute rejection from subjects with stable graft function and normal biopsy results. We calculated the area under the curve (AUC) and 95% confidence intervals for the AUC. The association between intragraft levels of mRNAs and miRNAs was analyzed using the Pearson regression, and the relationship between intragraft levels of miRNA or mRNA and renal allograft function was also analyzed using the Pearson regression. All data were expressed as mean±SE, unless otherwise specified. Statistical significance was tested by Student's t test or paired t test.
Based on the above disclosure, we identified that intragraft miRNA profiles distinguish patients with AR of human allografts from patients with normal allograft biopsy results, and that AR can be diagnosed with a high degree of accuracy with the use of intragraft levels of miRNAs. Moreover, miRNA profiles were also predictive of renal allograft function. Our observations, together, support the hypothesis that intragraft miRNA expression patterns may serve as biomarkers of human renal allograft status.
We used a 2-step approach to develop miRNA signatures predictive of AR. First, we ascertained intragraft expression patterns of 365 mature human miRNAs in 7 human renal allograft biopsies classified as AR or normal. Global expression profiling identified miRNAs differentially expressed in AR biopsies compared to normal biopsies (
Intragraft levels of miR-142-5p, -155, -223, -10b, -30a-3p, and let-7c predicted renal graft function with miR-142-5p and miR-10b showing the strongest association with graft function. Among the mRNAs analyzed, mRNA for CD3, but not mRNAs for CD20, NKCC-2, and USAG-1, predicted graft function, and the association between CD3 mRNA and graft function was weaker compared to that of miR-142-5p or miR-10b. Our observations that intragraft miRNA expression patterns are predictive of allograft status, in addition to the existing data that miRNAs are stable, present in high abundance, and can be examined in formalin-fixed tissues, advance the idea that miRNA expression patterns may be of value as biomarkers in clinical transplantation.
Several of the miRNAs found at a higher level in AR biopsies compared to normal allograft biopsies may play an important role in innate and adaptive immunity. Our in vitro studies showed that activation with the polyclonal T-cell mitogen PHA increases miR-155 expression in normal human PBMCs.
Intragraft levels of miR-146 were higher in AR samples compared to normal allograft biopsies. miR-146 is expressed at low levels in naïve T cells, is upregulated in Th1 cells, but not in Th2 cells, and is considered as a Th1-specific miRNA. In support of Th1-type cells infiltrating rejecting human renal allografts, we found that intragraft level of mRNA for the type 1 cytokine IFN-γ but not the level of mRNA for the Th2 cytokine 1L-4 were higher in AR biopsies compared to normal allograft biopsies (
Among the miRNAs overexpressed in the AR biopsies, miR-223 levels were the highest. We also found the abundance of miR-223 to be higher compared to that of miR-142-5p or miR-155 in normal human PBMCs, and that activation of PBMCs with PHA results in a reduction of miR-223 expression.
Intragraft levels of miR-142 were also higher in AR biopsies compared to normal allograft biopsies. We found that activation results in a reduction, albeit not statistically significant (P=0.08), in the expression of miR-142 in PBMCs.
Acute rejection of human renal allografts was also characterized by underexpression of miRNAs within the rejecting allografts compared to allografts with normal biopsy results. Indeed, among the 53 miRNAs differentially expressed between AR biopsies and normal biopsies, 43 were underexpressed and only 10 were overexpressed in the AR biopsies (
Two members of the let-7 family (let-7a and let-7c) were underexpressed in AR biopsies. Our investigation showed that let-7c is downregulated in PHA-activated PBMCs (
miR-30a-3p and miR-10b were both underexpressed in AR biopsies compared to normal allograft biopsies (
Urinary Cell Levels of miRNA 155 are diagnostic of acute rejection. Total RNA containing miRNAs was isolated from urinary cells collected from renal allograft recipients and levels of RNU44 (house keeping gene) and miRNA 155 were measured real time quantitative PCR assays. Urinary cell levels of miRNA 155 and not RNU 44 were significantly higher in urine from patients whose biopsies were classified acute rejection (n=3 specimens) compared to urine from patients with stable graft function and normal biopsy findings (n=13 specimens).
Incorporated herein by reference in its entirety is the Sequence Listing for the application. The Sequence Listing is disclosed on a computer-readable ASCII text file entitled, “Sequence_Listing_955_88PCTUS.txt”, created on Sep. 13, 2011. The sequence.txt file is 18 KB in size.
This application is a National Phase Application of International Application No. PCT/US2010/027361, filed on Mar. 15, 2010, which asserts priority to U.S. Provisional Application Ser. No. 61/160,188, filed on Mar. 13, 2009. Both aforementioned applications are hereby incorporated by reference in their entireties.
This invention was made with government support under grant numbers AI051652 and AI072790 awarded by the National Institutes of Health. The government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind | 371c Date |
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| PCT/US2010/027361 | 3/15/2010 | WO | 00 | 11/22/2011 |
| Publishing Document | Publishing Date | Country | Kind |
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| WO2010/105275 | 9/16/2010 | WO | A |
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| Number | Date | Country | |
|---|---|---|---|
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| Number | Date | Country | |
|---|---|---|---|
| 61160188 | Mar 2009 | US |
