Patent Application
20150167084
Allo-HSCT is a potentially curative treatment for a variety of hematologic diseases, including lymphoid and myeloid malignancies. Prior to transplantation, patients undergo conditioning with chemotherapy with or without irradiation, which results in severe immunodeficiency that particularly for the T-cell compartment can take months or years to restore1,2. This prolonged T-cell deficiency predisposes patients to infection and cancer relapse3-6. Strategies that improve T-cell reconstitution and recovery of high TCR diversity could therefore greatly reduce transplant-associated morbidity and mortality.
Restoration of TCR diversity after allo-HSCT heavily depends on the thymic generation of new naive T cells8-10. Thymic function, however, diminishes markedly after the onset of puberty, and, in the allo-HSCT setting, is further impaired due to conditioning-associated damage and graft-versus-host disease (GVHD)11,12. Thus, it is unclear how well TCR diversity can be restored, particularly in older patients using existing methods.
In a first set of embodiments, a method for determining T-cell receptorβ clonotype diversity and frequency in a subject includes obtaining a blood sample from the subject and isolating CD4+ and CD8+ T-lymphocytes, or subsets of CD4+ and CD8+ T-lymphocytes. The method further comprises extracting total RNA from the cells isolated, generating cDNA from the total RNA, amplifying the cDNA, and sequencing the amplified cDNA. The method still further includes identifying T-cell receptor β clonotypes in the cDNA sequences and quantifying the diversity of the clonotypes and the clonotype frequency of each clonotype in the sample.
In a second set of embodiments, a method for determining a change in T-cell receptor β clonotype diversity and frequency in a subject over time includes obtaining a first blood sample from the subject at a first time point and obtaining a second blood sample at a second later time point. The method also includes isolating CD4+ and CD8+ T-lymphocytes or subsets of the CD4+ and CD8+ T-lymphocytes from each sample. The method further includes extracting total RNA from the cells isolated for each sample, generating cDNA from the total RNA for each sample, amplifying the cDNA for each sample, and sequencing the amplified cDNA for each sample. The method still further includes identifying T-cell receptor β clonotypes in the cDNA sequences and quantifying the diversity of the clonotypes and frequency of each clonotype in each sample. The method yet further includes determining, based on at least one of the diversity of the clonotypes in each sample or the frequency of at least one clonotype in each sample, whether there is a statistically significant increase in T-cell receptor β clonotype diversity or frequency at the second time point, or whether T-cell receptor β clonotype diversity or frequency is not statistically significantly changed at the second time point, or whether there is a statistically significant decrease in T-cell receptor β clonotype diversity or frequency at the second time point.
Unless otherwise specifically defined herein, terms and symbols of nucleic acid chemistry, biochemistry, genetics, and molecular biology used herein follow those of standard treatises and texts in the field, e.g. Kornberg and Baker, DNA Replication. Second Edition (W.H. Freeman. N.Y., 1992); Lehninger, Biochemistry. Second Edition (Worth Publishers. New York, 1975): Strachan and Read. Human Molecular Genetics. Second Edition (Wiley-Liss, New York, 1999); Abbas et al, Cellular and Molecular Immunology, 6.sup.th edition (Saunders, 2007).
As used herein, “nucleic acid” means DNA, RNA and derivatives thereof. In some embodiments, the nucleic acid is single stranded. Modifications include, but are not limited to, those which provide other chemical groups that incorporate additional charge, polarizability, hydrogen bonding, electrostatic interaction, and functionality to the nucleic acid ligand bases or to the nucleic acid ligand as a whole. Such modifications include, but are not limited to, phosphodiester group modifications (e.g., phosphorothioates, phosphorodithioates, boranophosphonates, methylphosphonates), 2′-position sugar modifications, 5-position pyrimidine modifications, 8-position purine modifications, modifications at exocyclic amines, substitution of 4-thiouridine, substitution of 5-bromo or 5-iodo-uracil; backbone modifications, methylations, unusual base-pairing combinations such as the isobases isocytidine and isoguanidine and the like. Modifications can also include 3′ and 5′ modifications such as capping moieties. A 2′ deoxy nucleic acid linker is a divalent nucleic acid compound of any appropriate length and/or internucleotide linkage wherein the nucleotides are 2′ deoxy nucleotides.
The terms “DNA” and “RNA” refer to deoxyribonucleic acid and ribonucleic acid, respectively.
Where a method disclosed herein refers to “amplifying” a nucleic acid, the term “amplifying” refers to a process in which the nucleic acid is exposed to at least one round of extension, replication, or transcription in order to increase (e.g., exponentially increase) the number of copies (including complimentary copies) of the nucleic acid. The process can be iterative including multiple rounds of extension, replication, or transcription. Various nucleic acid amplification techniques are known in the art, such as PCR amplification or rolling circle amplification.
A “primer” as used herein refers to a nucleic acid that is capable of hybridizing to a complimentary nucleic acid sequence in order to facilitate enzymatic extension, replication or transcription.
“Complementary,” as used herein, refers to the capacity for precise pairing of two nucleobases (e.g., A to T (or U), and G to C) regardless of where in the nucleic acid the two are located. For example, if a nucleobase at a certain position of nucleic acid is capable of hydrogen bonding with a nucleobase at a certain position of another nucleic acid, then the position of hydrogen bonding between the two nucleic acids is considered to be a complementary position. Nucleic acids are “substantially complementary” to each other when a sufficient number of complementary positions in each molecule are occupied by nucleobases that can hydrogen bond with each other. Thus, the term “substantially complementary” is used to indicate a sufficient degree of precise pairing over a sufficient number of nucleobases such that stable and specific binding occurs between the nucleic acids. The phrase “substantially complementary” thus means that there may be one or more mismatches between the nucleic acids when they are aligned, provided that stable and specific binding occurs. The term “mismatch” refers to a site at which a nucleobase in one nucleic acid and a nucleobase in another nucleic acid with which it is aligned are not complementary. The nucleic acids are “perfectly complementary” to each other when they are fully complementary across their entire length.
The phrase “amino acid” as used herein refers to any of the twenty naturally occurring amino acids as well as any modified amino acids. Modifications can include natural processes such as posttranslational processing, or chemical modifications which are known in the art. Modifications include, but are not limited to, phosphorylation, ubiquitination, acetylation, amidation, glycosylation, covalent attachment of flavin, ADP-ribosylation, cross linking, iodination, methylation, and the like.
The words “protein”, “peptide”, and “polypeptide” are used interchangeably to denote an amino acid polymer or a set of two or more interacting or bound amino acid polymers. Rapid Amplification of cDNA Ends (RACE) is a technique used in molecular biology to obtain the full length sequence of an RNA transcript found within a cell. RACE results in the production of a cDNA copy of the RNA sequence of interest, produced through reverse transcription, followed by PCR amplification of the cDNA copies (see RT-PCR). The amplified cDNA copies are then sequenced and, if long enough, should map to a unique mRNA already described, the full sequence of which is known. RACE can provide the sequence of an RNA transcript from a small known sequence within the transcript to the 5′ end (5′ RACE-PCR). The first step in RACE is to use reverse transcription to produce a cDNA copy of a region of the RNA transcript. In this process, an unknown end portion of a transcript is copied using a known sequence from the center of the transcript. The copied region is bounded by the known sequence, and either the 5′ or 3′ end. 5′ RACE-PCR begins using mRNA as a template for a first round of cDNA synthesis (or reverse transcription) reaction using an anti-sense (reverse) oligonucleotide primer that recognizes a known sequence in the gene of interest; the primer is called a gene specific primer (GSP), and it copies the mRNA template in the 3′ to the 5′ direction to generate a specific single-stranded cDNA product. Following cDNA synthesis, the enzyme terminal deoxynucleotidyl transferase (TdT) is used to add a string of identical nucleotides, known as a homopolymeric tail, to the 3′ end of the cDNA. (There are some other ways to add the 3′-terminal sequence for the first strand of the de novo cDNA synthesis which are much more efficient than homopolymeric tailing, but the sense of the method remains the same). A PCR reaction is then carried out, which uses a second anti-sense gene specific primer (GSP2) that binds to the known sequence, and a sense (forward) universal primer (UP) that binds the homopolymeric tail added to the 3′ ends of the cDNAs to amplify a cDNA product from the 5′ end.
“Deep sequencing” is used herein in conformity with the ordinary meaning of the term in the art, i.e., high-throughput sequencing methodology such as the massively parallel sequencing methodologies for example using Illumina and Roche/454. Deep sequencing can analyze tens of millions of reads in parallel.
“Clonality” as used herein means a measure of the degree to which the distribution of clonotype abundances among clonotypes of a repertoire is skewed to a single or a few clonotypes. Roughly, clonality is an inverse measure of clonotype diversity.
“Clonotype” means a recombined nucleotide sequence of a T cell encoding a T cell receptor (TCR), or a portion thereof. In one aspect, a collection of all the distinct clonotypes of a population of lymphocytes of an individual is a repertoire of such population, e.g. Arstila et al. Science, 286: 958-961 (1999); Yassai et al. Immunogenetics, 61: 493-502 (2009); Kedzierska et al, Mol. Immunol., 45(3): 607-618 (2008); and the like. In one aspect, clonotypes of a repertoire comprises any segment of nucleic acid common to a T cell population which has undergone somatic recombination during the development of TCRs, including normal or aberrant (e.g. associated with cancers) precursor molecules thereof, including, but not limited to any of the following: an immunoglobulin heavy chain (IgH) or subsets thereof (e.g. an IgH variable region, CDR3 region, or the like), incomplete IgH molecules, an immunoglobulin light chain or subsets thereof (e.g. a variable region, CDR region, or the like). T cell receptor .alpha. chain or subsets thereof, T cell receptor .beta. chain or subsets thereof (e.g. variable region, CDR3, V(D)J region, or the like), a CDR (including CDR1, CDR2 or CDR3, of either TCRs or BCRs, or combinations of such CDRs). V(D)J regions of either TCRs or BCRs, hypermutated regions of IgH variable regions, or the like.
As used herein, “clonotype profile.” or “repertoire profile,” is a tabulation of clonotypes of a sample of T cells (such as a peripheral blood sample containing such cells) that includes substantially all of the repertoire's clonotypes and their relative abundances. “Clonotype profile,” “repertoire profile,” and “repertoire” are used herein interchangeably. The term “repertoire,” means a repertoire measured from a sample of T lymphocytes). In one aspect of the invention, clonotypes comprise portions of a TCRβ. chain. In other aspects of the invention, clonotypes may be based on other recombined molecules, such as immunoglobulin light chains or TCR.alpha chains, or portions thereof.
“Repertoire”, or “immune repertoire”, means a set of distinct recombined nucleotide sequences that encode T cell receptors (TCRs), or fragments thereof, in a population of T-lymphocytes of an individual, wherein the nucleotide sequences of the set have a one-to-one correspondence with distinct lymphocytes or their clonal subpopulations for substantially all of the lymphocytes of the population. In one aspect, a population of lymphocytes from which a repertoire is determined is taken front one or more tissue samples, such as one or more blood samples.
“Immunosuppression” can occur in, for example, malnutrition, aging, many types of cancer (such as leukemia, lymphoma, multiple myeloma), sepsis and certain chronic infections such as acquired immunodeficiency syndrome (HIV/AIDS). The unwanted effect in immunosuppression is immunodeficiency that results in increased susceptibility to pathogens such as bacteria and virus. In the context of the present invention “immunodeficiency” or “immune compromised/immunocompromised” are used interchangeably and refer to T-cell deficiencies that cause the disorders. These include marrow and other transplants, AIDS, HIV, Cancer chemotherapy, lymphoma and subjects undergoing glucocorticoid therapy, infections caused by intracellular pathogens including Herpes simplex virus, Mycobacterium, Listeria, and intracellular fungal infections. A person who has an immunodeficiency of any kind is said to be immunocompromised. An immunocompromised person may be particularly vulnerable to opportunistic infections, in addition to normal infections that could affect everyone.
Autoimmune diseases include but are not limited to the following: Acute Disseminated Encephalomyelitis (ADEM); Acute necrotizing hemorrhagic leukoencephalitis; Addison's disease; Agammaglobulinemia; Alopecia areata; Amyloidosis; Ankylosing spondylitis; Anti-GBM/Anti-TBM nephritis; Antiphospholipid syndrome (APS); Autoimmune angioedema; Autoimmune aplastic anemia; Autoimmune dysautonomia; Autoimmune hepatitis; Autoimmune hyperlipidemia; Autoimmune immunodeficiency; Autoimmune inner ear disease (AIED); Autoimmune myocarditis; Autoimmune oophoritis; Autoimmune pancreatitis; Autoimmune retinopathy; Autoimmune thrombocytopenic purpura (ATP); Autoimmune thyroid disease; Autoimmune urticarial; Axonal & neuronal neuropathies; Balo disease; Behcet's disease; Bullous pemphigoid; Cardiomyopathy; Castleman disease; Celiac disease; Chagas disease; Chronic fatigue syndrome**; Chronic inflammatory demyelinating polyneuropathy (CIDP); Chronic recurrent multifocal ostomyelitis (CRMO); Churg-Strauss syndrome; Cicatricial pemphigoid/benign mucosal pemphigoid; Crohn's disease; Cogans syndrome; Cold agglutinin disease; Congenital heart block; Coxsackie myocarditis; CREST disease; Essential mixed cryoglobulinemia; Demyelinating neuropathies; Dermatitis herpetiformis; Dermatomyositis; Devic's disease (neuromyelitis optica); Discoid lupus; Dressler's syndrome; Endometriosis; Eosinophilic esophagitis; Eosinophilic fasciitis; Erythema nodosum; Experimental allergic encephalomyelitis; Evans syndrome; Fibromyalgia**; Fibrosing alveolitis; Giant cell arteritis (temporal arteritis); Giant cell myocarditis; Glomerulonephritis; Goodpasture's syndrome; Granulomatosis with Polyangiitis (GPA) (formerly called Wegener's Granulomatosis); Graves' disease; Guillain-Barre syndrome; Hashimoto's encephalitis; Hashimoto's thyroiditis; Hemolytic anemia; Henoch-Schonlein purpura; Herpes gestationis; Hypogammaglobulinemia; Idiopathic thrombocytopenic purpura (ITP); IgA nephropathy; IgG4-related sclerosing disease; Immunoregulatory lipoproteins; Inclusion body myositis; Interstitial cystitis; Juvenile arthritis; Juvenile diabetes (Type 1 diabetes); Juvenile myositis; Kawasaki syndrome; Lambert-Eaton syndrome; Leukocytoclastic vasculitis; Lichen planus; Lichen sclerosus; Ligneous conjunctivitis; Linear IgA disease (LAD); Lupus (SLE); Lyme disease, chronic; Meniere's disease; Microscopic polyangiitis; Mixed connective tissue disease (MCTD); Mooren's ulcer; Mucha-Habermann disease; Multiple sclerosis; Myasthenia gravis; Myositis; Narcolepsy; Neuromyelitis optica (Devic's); Neutropenia; Ocular cicatricial pemphigoid; Optic neuritis; Palindromic rheumatism; PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus); Paraneoplastic cerebellar degeneration; Paroxysmal nocturnal hemoglobinuria (PNH); Parry Romberg syndrome; Parsonnage-Turner syndrome; Pars planitis (peripheral uveitis); Pemphigus; Peripheral neuropathy; Perivenous encephalomyelitis; Pernicious anemia; POEMS syndrome; Polyarteritis nodosa; Type I, II, & III autoimmune polyglandular syndromes; Polymyalgia rheumatic; Polymyositis; Postmyocardial infarction syndrome; Postpericardiotomy syndrome; Progesterone dermatitis; Primary biliary cirrhosis; Primary sclerosing cholangitis; Psoriasis; Psoriatic arthritis; Idiopathic pulmonary fibrosis; Pyoderma gangrenosum; Pure red cell aplasia; Raynauds phenomenon; Reactive Arthritis; Reflex sympathetic dystrophy; Reiter's syndrome; Relapsing polychondritis; Restless legs syndrome; Retroperitoneal fibrosis; Rheumatic fever; Rheumatoid arthritis; Sarcoidosis; Schmidt syndrome; Scleritis; Scleroderma; Sjogren's syndrome; Sperm & testicular autoimmunity; Stiff person syndrome; Subacute bacterial endocarditis (SBE); Susac's syndrome; Sympathetic ophthalmia; Takayasu's arteritis; Temporal arteritis/Giant cell arteritis; Thrombocytopenic purpura (TTP); Tolosa-Hunt syndrome; Transverse myelitis; Type 1 diabetes; Ulcerative colitis; Undifferentiated connective tissue disease (UCTD); Uveitis; Vasculitis; Vesiculobullous dermatosis; Vitiligo; and Wegener's granulomatosis (now termed Granulomatosis with Polyangiitis (GPA).
Delayed T-cell recovery and restricted T-cell receptor (TCR) diversity after allogeneic hematopoietic stem cell transplantation (allo-HSCT) are related to the increased risks of infection and cancer relapse. Measuring T-cell receptor diversity is challenging and generally requires numerous molecular assays that must be performed in parallel in order to obtain a rough estimate of the receptor repertoire. A simple and rapid method that enables T-cell receptor repertoire determination is needed.
New methods for determining T-cell receptor β clonotype diversity and frequency have been discovered that permit 1) a comparison of the clonotype diversity between a subject having a disease associated with immunosuppression or immunodeficiency (such as in a subject that has received an allo-HSCT) or an autoimmune disease and a healthy subject, 2) monitoring recovery of T-cell receptor β clonotype diversity in an immunosuppressed subject such as a cancer patient, to identify, inter alia, subjects at risk of cancer relapse, 3) determining if a therapeutic regimen is causing an increase or decrease or no change in clonogype diversity and frequency over the course of therapy as a way to determine treatment efficacy, and 4) screening test agents to identify a test agent that increases T-cell receptor β clonotype diversity. A summary of these and other new methods is set forth in the Summary of the Invention.
Over the past two decades, several strategies have been developed to probe human TCR diversity. One strategy aims to identify the presence of different TCR families, by using flow cytometry or PCR to determine the usage of different TCR variable (V) genes13,14. A second strategy, called CDR3 size spectratyping, aims to determine polyclonality of the repertoire, by using fluorescent primers to measure length variation of the CDR3 region within each TCR V family15,16. Spectratyping in particular has been useful to document substantial abnormalities in T-cell repertoire composition after allo-HSCT17-19. However, as neither of these strategies is able to measure the frequency of individual TCRs, they can only provide an estimate of repertoire complexity. With the advent of deep sequencing technology, it has now become possible to directly measure TCR diversity with high resolution20-26. Embodiments of the present invention incorporate deep sequencing to address two fundamental questions related to T-cell reconstitution after allo-HSCT: how TCR diversity recovers I) over time and II) as a function of different stem cell sources (i.e. different types of transplants)27,28.
Embodiments of the invention are directed to a method to reproducibly and accurately measure human TCR diversity. In an embodiment 5′-RACE PCR is combined with deep sequencing, to assess the entire TCR receptor β repertoire using a single oligonucleotide pair, thereby eliminating amplification bias. This contrasts with TCR sequencing methods based on gDNA20-23, which have to use many different oligonucleotides for amplification, making some degree of bias unavoidable. While 5′-RACE PCR provides a clear advantage, a limitation is that it requires RNA, and thus changes in TCR transcription could skew the frequency of particular clonotypes. Although Roche/454 sequencing was used in the Examples herein, the new methods can be readily adaptable to other platforms with greater sequence coverage, which could help to identify infrequent TCRs. The Illumina MiSeq platform provides deeper sequencing capacity, with the ability to determine T-cell receptor diversity and the presence of T cell clonotypes in individuals with a broad repertoire.
Experiments were conducted to determine T-cell repertoire recovery in allo-HSCT recipients over time, in whom limited TCR diversity is linked to susceptibility to infection and cancer relapse. Although significant improvement in TCR diversity in allo-HSCT subjects over time, there was substantial variability in the rate of recovery between different stem cell sources, including DUCB, TCD and unmanipulated peripheral blood stem cell transplants. Most notably, DUCB recipients had a 28-fold higher CD4+ T-cell diversity compared to TCD recipients after 6 months. It is important to note that this is consistent with clinical findings, which have shown that after 6 months, DUCB recipients have a low incidence of infection,33 higher CD4+ T-cell numbers and a lower rate of leukemia relapse27 than TCD recipients.33,34 Although many variables could contribute to this differential repertoire recovery, at least partially it can be explained by the fact that DUCB recipients receive ˜7,000-fold more T cells in their graft and transplantation is performed without T-cell-depleting regimens.33
Besides allo-HSCT, this method should be useful to characterize T-cell immunity in other clinical settings of immune deficiency, autoimmunity and tumor immunity. Ultimately, the ability to measure T-cell repertoire complexity with great precision should guide the way for novel therapeutic approaches aimed at immune regeneration. Hence certain embodiments are directed to screening test agents to identify those that increase T cell diversity in cultured T cells (CD4 and CD8) taken from an immunosuppressed subject.
T cells typically express only one TCRβ chain, making sequence analysis of TCRβ cDNA a useful measure of TCR diversity. However, in some embodiments T cell diversity is measured by sequence analysis of TCRalpha or Igg.
Analysis of the TCRβ repertoire following T-cell-depleted (TCD) peripheral blood stem cell transplantation (TCD) was highly reproducible using 5′-RACE PCR, which amplified all 48 Vβ genes using a single oligonucleotide pair. See Table 1 which shows that the entire TCRβ repertoire was covered.
Comparison of two blood samples from a single TCB transplant patient (TCB #1) showed a highly reproducible pattern of Vβ usage, which differed markedly from healthy subjects (
Analysis of the TCB #1 patient's repertoire at 138 days after transplant revealed a very low TCR diversity (1/Ds: 23), which was more than 100-fold lower than the average diversity of four healthy subjects (1/Ds: 2,525;
Despite profound changes in repertoire composition, TCR diversity did not increase over time (1/Ds: 23 and 19 for days 138 and 377, respectively;
TCR diversity in 27 patients at either 6 or 12 months after conventional (Conv) or TCD peripheral blood stem cell transplantation, or double-unit umbilical cord blood (DUCB) transplantation (
I) For all stem cell sources as well as for healthy subjects, CD4+ T-cell diversity was ˜50-times higher than CD8+ T-cell diversity (1/Ds: 4,665 and 81, respectively;
II) DUCB recipients had the highest TCR diversity of all patients and had a significantly (28-fold; P=0.033) more diverse CD4+ T-cell repertoire compared to TCD recipients after 6 months. Importantly, this increased TCR diversity also correlated with a substantially greater fraction of naïve CD4+ T cells in DUCB compared to TCD recipients (
No significant impact of age or donor on TCR diversity (
Within each stem cell group, patients were identified who had normal T-cell counts, but very low TCR diversity after one year (
The CD4+ T-cell and CD8+ T-cell repertoires were stable over time (19-21 months) in of certain transplant patients [CD4+ T-cell: Conv #6 and TCD #8; and CD8+ T-cell: DUCB #7] as well as in healthy subjects.
Patients.
28 patients with various hematologic malignancies underwent allo-HSCT at Memorial Sloan-Kettering Cancer Center (MSKCC) from April 2010 through September 2011. Patient and treatment characteristics are summarized in Table 1. Pre-transplant conditioning varied according to the patient's age, diagnosis, remission status, extent of prior therapies, and co-morbidities; and consisted of high-dose, reduced-intensity myeloablative and nonmyeloablative regimens31. GVHD prophylaxis for peripheral blood stem cell transplantation was either with T-cell depletion32 or calcineurin inhibitor-based, and ATG was used according to protocol or physician preference. Cord blood recipients received mycophenolate mofetil and calcineurin inhibitors; however, no patient received ATG30. Post-transplant granulocyte colony-stimulating factor (G-CSF)33 was used in all patients. Acute and late acute/chronic GVHD were diagnosed clinically with histological confirmation when possible. Staging of acute GVHD was graded according to CIBMTR criteria34. Blood samples were obtained by venipuncture after written informed consent under MSKCC protocol 08-047.
T-Cell Isolation and Flow Cytometry.
From each ˜8 ml heparinized blood sample, mononuclear cells were isolated by Ficoll density centrifugation (Lymphocyte Separation Medium, MP Biomedicals). Recovered cells were lysed in RLT buffer (QIAGEN), homogenized using QIAshredder columns (QIAGEN) and stored at −80° C. until further use. For CD4+ and CD8+ T-cell separation, two ˜8 ml heparinized blood samples were pooled, followed by isolation of the mononuclear cell fraction as above. Recovered cells were split into two fractions and incubated with either human CD4 or CD8 MicroBeads (Miltenyi Biotec). CD4+ and CD8+ T cells were separated using MS columns (Miltenyi Biotec). Eluted cells were lysed, homogenized and stored as above. To determine the efficiency of T-cell separation, eluted cells were stained with FITC anti-human CD14 (clone M5E2), PE-Cy7 anti-human CD4 (clone SK3) and APC anti-human CD8 (clone RPA-T8; all BD Pharmingen); and measured on an LSRII flow cytometer (BD Biosciences). Data was analyzed using FlowJo software (TreeStar). For separation of naïve and memory CD8+ T-cells, isolated mononuclear cells were stained with FITC anti-human CD45RA (clone HI100), PE anti-human CD45RO (clone UCHL1; both BD Pharmingen) and APC anti-human CD8. Cells were sorted using a FACSAria cell sorter (BD Biosciences) into CD8+CD45RA+CD45RO− (naïve) and CD8+CD45RA−CD45RO+ (memory) fractions.
5′-Race PCR and Roche/454 Sequencing.
Total RNA from frozen homogenates was extracted using an RNeasy mini kit (QIAGEN). RACE-Ready cDNA was generated using a SMARTer RACE cDNA Amplification kit (Clontech) and oligo(dT) or random (N-15) primers. 5′-RACE PCR was performed using Advantage 2 Polymerase mix (Clontech) with Clontech's universal forward primer and a self-designed universal TCRβ-constant reverse primer compatible with both human TRBC gene segments (5′-GCACACCAGTGTGGCCTTTTGGG-3′ SEQ ID NO. 6). Amplification was performed on a Mastercycler pro (Eppendorf) and was 1 min at 95° C.; 5 cycles of 20 sec at 95° C. and 30 sec at 72° C.; 5 cycles of 20 sec at 95° C., 30 sec at 70° C. and 30 sec at 72° C.; 25 cycles of 20 sec at 95° C., 30 sec at 60° C. and 30 sec at 72° C.; 7 min at 72° C. PCR products were loaded on 1.2% agarose gels (Bio-Rad) and bands centered at ˜600 bp were excised and purified using a MinElute Gel Extraction kit (QIAGEN). Purified products were subjected to a second round of amplification to introduce adaptor sequences compatible with unidirectional Roche/454 sequencing. 1/50th of first-round PCR product was amplified using Advantage 2 Polymerase mix with a hybrid forward primer consisting of Roche's Lib-L primer B and Clontech's nested universal primer (5′-CCTATCCCCTGTGTGCCTTGGCAGTCTCAGAAGCAGTGGTATCAACGCAGAGT-3 SEQ ID NO. 7′) and a hybrid reverse primer consisting of Roche's Lib-L primer A and a self-designed nested universal TCRβ-constant primer (5′-CCATCTCATCCCTGCGTGTCTCCGACTCAG-MID-AACACAGCGACCTCGGGTGGGAA-3′ SEQ ID NO. 8), wherein MID represents the multiplex identifier used to separate pooled samples during sequence analysis). The multiplex identifier is essentially a bar code that is added to primers so that multiple samples can be resolved after high throughput sequences of a mixture of samples. Multiplex identifiers were 6-7 bp long. Amplification was 1 min at 95° C.; 25 cycles of 20 sec at 95° C., 30 sec at 68° C. and 30 sec at 72° C.; 7 min at 72° C. PCR products were purified from agarose gels as above. Purified products were measured, pooled and sequenced using the GS Junior 454 platform (Roche) following the manufacturer's instructions.
Sequence Data Analysis.
Raw sequence data was converted to FASTA format using MOTHUR software35. Sequences shorted than 125 bp, with uncalled bases, with a Phred quality score average below 30 (base call accuracy <99.9%)27, or with no exact match to the TCRβ-constant primer or a multiplex identifier were discarded. Resulting FASTA files were uploaded to the IMGT/HighV-QUEST database (http://www.imgt.org/HighV-QUEST/index.action)36. Using IMGT summary files, sequences with out-of-frame rearrangements, with a V- and J-region identity <80%, with V-region pseudogenes or a CDR3β AA junction lacking a 5′ cysteine and 3′ phenylalanine were discarded. Resulting sequences were sorted using Excel (Microsoft) and graphed using Prism 5 software (GraphPad). The inverse Simpson's diversity index (1/Ds) was calculated using MOTHUR.
Statistical Analysis.
TCR diversity was compared using an unpaired Student's t-test (two groups) or one-way ANOVA with Bonferroni's multiple comparison test (three groups). A P-value of <0.05 was considered statistically significant.
T cells typically express only one productively recombined TCRβ chain, making sequence analysis of TCRβ cDNA a useful measure of T-cell repertoire complexity. To evaluate the human TCRβ repertoire in a faithful manner, use was mad of 5′ rapid amplification of cDNA ends (RACE), which allows amplification of all 48 different Vβ genes using a single oligonucleotide pair. Other amplification methods can be used in the methods of the invention.
To test the reproducibility of this approach, separately amplified were two ˜8 ml blood samples that were obtained from a single patient TCD #1, after written informed consent, 138 days following T-cell-depleted (TCD) peripheral blood stem cell transplantation (TCD #1; Table 1). Since the T-cell repertoire of this patient was likely severely restricted, also separately amplified were two blood samples from each of four healthy subjects (Healthy #1-4; Table 1), to serve as a reference for normal high TCR diversity. Following amplification, all samples were analyzed by Roche/454 sequencing or Illumina MiSeq, using a Phred quality score average of 30 to minimize the contribution of sequence errors27. Among total TCR sequences, all 48 different Vβ genes were found in the subjects_(
Next, the frequency was determined at which each distinct TCRβ chain, or TCRβ clonotype, was present among the total pool of TCRs. In 15,902 reads obtained from both blood samples of the TCD #1, 1,097 distinct TCRβ clonotypes, were detected with the most frequent clonotype comprising 11.7% of the total repertoire (
To establish how accurately the frequency of individual clonotypes had been determined, the clonotype distribution of both blood samples from TCD #1 were compared. Importantly, abundant clonotypes found in TCD #1 blood sample were found with almost identical frequency in the second blood sample (also from TCD #1), resulting in a near-perfect correlation of both clonotype distributions (r: 0.98;
To provide a quantitative value for TCR diversity, the inverse Simpson's diversity index (1/Ds) was used, which sums the fraction each clonotype makes up of the total repertoire28. This index ranges from 1 (no diversity) to ∞ (infinite diversity) and is highest when all clonotypes have an equal distribution. To test the usefulness of this index, naïve and memory CD8+ T cells from Healthy #1 were sorted and a 20-fold higher TCR diversity found in the naïve T-cell compartment compared to the memory CD8+ cells (
Previous studies have suggested a considerable lag time in the restoration of thymic activity after allo-HSCT8,10. Based the observation that individual clonotypes can comprise as much as 10% of the repertoire 4.5 months after transplant, it is speculated that over time such clonotypes should be diluted out by the addition of recent thymic emigrants, driving the repertoire towards a more even distribution9.
To monitor repertoire recovery over time, three additional timepoints of TCD no. 1 were measured at days 147, 194 and 377 after transplant. To our surprise, TCR Vβ usage was very different at each timepoint examined (
Given that the presented method allows accurate characterization of human T-cell repertoires, a method was developed to stratify allo-HSCT recipients according to their TCR diversity, thereby enabling identification of patients with particularly narrow T-cell repertoires. As a first step, TCR diversity was measured in recipients of three different stem cell sources at two different time points25. To this end, 27 cancer patients who received transplants were sequenced at either 6 or 12 months after either conventional (Conv) or T-cell-depleted (TCD) peripheral blood stem cell transplantation, or double-unit umbilical cord blood (DUCB) transplantation without anti-thymocyte globulin30 (Table 1,
Analysis of total TCR sequences indicated that Vβ gene usage between both T-cell compartments followed markedly distinct patterns (
Next, the clonotype distribution of the individual CD4+ and CD8+ T-cell repertoires were determined for the 27 transplant patients.
After determining the TCR diversity of each individual, it was established that: I) for all stem cell sources as well as for healthy donors, CD4+ T-cell diversity was ˜50-times higher than CD8+ T-cell diversity (1/Ds: 4,665 and 81, respectively;
Using above data, several clinical parameters were investigated that could influence T-cell repertoire recovery. No significant impact was found of age or donor on TCR diversity (
Using above data, several clinical parameters were investigated that could influence T-cell repertoire recovery. No significant impact was found of age or donor on TCR diversity (
Within each stem cell group, patients were identified who had normal T-cell counts, but very low TCR diversity after one year (Supplementary
In this study, a methodology is established to measure human TCR diversity in a reproducible and quantitative way. By combining 5′-RACE PCR of TCRβ cDNA with deep sequencing, this method allows assessment of the entire human TCRβ repertoire using a single oligonucleotide pair for amplification. This method was validated by measuring T-cell repertoire recovery in allo-HSCT recipients, in whom limited TCR diversity is linked to susceptibility to infection and cancer relapse. Overall, significant improvement was found in TCR diversity between 6 and 12 months after transplant, providing proof-of-principle that the presented method can document T-cell repertoire recovery. However, there was substantial variability in the rate of repertoire recovery by different stem cell sources. Interestingly, cord blood recipients demonstrated superior TCR diversity over peripheral blood stem cell recipients, and approximated the TCR diversity of healthy subjects by 6 months. It is important to note that all cord blood transplantations are performed without the inclusion of anti-thymocyte globulin (ATG) in the preparative regimen, and this has recently been shown to be associated with a ˜3.5-fold faster T-cell recovery after 6 months compared to ATG-based cord blood transplantation30. Next to differences in transplant conditions, also identified were individual patients that had normal T-cell counts after 12 months, but 25- to 150-fold lower TCR diversity compared to their group mean. After 18 months, TCR diversity of one of these patients had improved substantially but that of others had not, illustrating the use of this method to gauge an individual patient's immunocompetence.
Although applied here in the setting of T-cell reconstitution after allo-HSCT, this method can be used to determine TCR diversity in a variety of immune diseases, such as HIV/AIDS and autoimmunity. Ultimately, the ability to monitor T-cell repertoire recovery with great precision provides new methods to identify agents that increase T cell repertoire recovery and immune regeneration.
First round of PCR amplification
MID represents the multiplex identifier used to separate pooled samples during sequence analysis. Multiplex identifiers were 6-7 bp long.
As described herein, the present methods can be used in conjunction with a variety of sequencing techniques. In some embodiments, the process to determine the nucleotide sequence of a target nucleic acid can be an automated process.
Templates (e.g., nucleic acids and fragments thereof) may be amplified on beads, for example using emulsion PCR methods. In order to use emulsion based amplification techniques with a single template per emulsion bubble, a single primer is attached to the bead, and a single primer is in solution, thereby amplifying the templates such that one end of the duplex is attached to the bead. The hybridized strand can be removed by denaturing the duplex, thereby leaving the immobilized single strand on the bead. The single stranded templates can be captured onto a surface via primers complementary to the templates. Exemplary emulsion-based amplification techniques that can be used in a method of the invention are described in US 2005/0042648; US 2005/0079510; US 2005/0130173 and WO 05/010145, each of which is incorporated herein by reference in its entirety and for all purposes.
Templates can be amplified on a surface using bridge amplification to form nucleic acid clusters. Bridge amplification gives a double stranded template where both ends are immobilized. Methods of generating nucleic acid clusters for use in high-throughput nucleic acid technologies have been described, as noted above. See, for example, U.S. Pat. No. 7,115,400, U.S. Patent Application Publication Nos. 2005/0100900 and 2005/0059048, and PCT Publication Nos. WO 98/44151, WO 00/18957, WO 02/46456, WO 06/064199, and WO 07/010,251, each of which is incorporated by reference herein in its entirety and for all purposes.
Some embodiments include sequencing by synthesis (SBS) techniques. SBS techniques generally involve the enzymatic extension of a nascent nucleic acid strand through the iterative addition of nucleotides or oligonucleotides against a template strand. In traditional methods of SBS, a single nucleotide monomer may be provided to a target nucleotide in the presence of a polymerase in each delivery.
SBS can utilize nucleotide monomers that have a terminator moiety or those that lack any terminator moieties. Methods utilizing nucleotide monomers lacking terminators include, for example, pyrosequencing and sequencing using .gamma.-phosphate-labeled nucleotides. In methods using nucleotide monomers lacking terminators, the number of different nucleotides added in each cycle can be dependent upon the template sequence and the mode of nucleotide delivery. For SBS techniques that utilize nucleotide monomers having a terminator moiety, the terminator can be effectively irreversible under the sequencing conditions used as is the case for traditional Sanger sequencing which utilizes dideoxynucleotides, or the terminator can be reversible as is the case for sequencing methods developed by Solexa (now Illumina, Inc.). In preferred methods a terminator moiety can be reversibly terminating.
SBS techniques can utilize nucleotide monomers that have a label moiety or those that lack a label moiety. Accordingly, incorporation events can be detected based on a characteristic of the label, such as fluorescence of the label; a characteristic of the nucleotide monomer such as molecular weight or charge; a byproduct of incorporation of the nucleotide, such as release of pyrophosphate; or the like. In embodiments, where two or more different nucleotides are present in a sequencing reagent, the different nucleotides can be distinguishable from each other. For example, the different nucleotides present in a sequencing reagent can have different labels and they can be distinguished using appropriate optics as exemplified by the sequencing methods developed by Solexa (now Illumina, Inc.).
Some embodiments include pyrosequencing techniques. Pyrosequencing detects the release of inorganic pyrophosphate (PPi) as particular nucleotides are incorporated into the nascent strand (Ronaghi, M., Karamohamed, S., Pettersson, B., Uhlen, M. and Nyren, P. (1996) “Real-time DNA sequencing using detection of pyrophosphate release.” Analytical Biochemistry 242(1):84-9; Ronaghi, M. (2001) “Pyrosequencing sheds light on DNA sequencing.” Genome Res. 11(1):3-11; Ronaghi, M., Uhlen, M. and Nyren, P. (1998) “A sequencing method based on real-time pyrophosphate.” Science 281(5375):363; U.S. Pat. No. 6,210,891; U.S. Pat. No. 6,258,568 and U.S. Pat. No. 6,274,320, the disclosures of which are incorporated herein by reference in their entireties and for all purposes). In pyrosequencing, released PPi can be detected by being immediately converted to adenosine triphosphate (ATP) by ATP sulfurylase, and the level of ATP generated is detected via luciferase-produced photons.
In another example type of SBS, cycle sequencing is accomplished by stepwise addition of reversible terminator nucleotides containing, for example, a cleavable or photobleachable dye label as described, for example, in U.S. Pat. No. 7,427,67, U.S. Pat. No. 7,414,163 and U.S. Pat. No. 7,057,026, the disclosures of which are incorporated herein by reference and for all purposes. This approach is being commercialized by Solexa (now Illumina Inc.), and is also described in WO 91/06678 and WO 07/123,744 (filed in the United States patent and trademark Office as U.S. Ser. No. 12/295,337), each of which is incorporated herein by reference in their entireties and for all purposes. The availability of fluorescently-labeled terminators in which both the termination can be reversed and the fluorescent label cleaved facilitates efficient cyclic reversible termination (CRT) sequencing. Polymerases can also be co-engineered to efficiently incorporate and extend from these modified nucleotides.
Additional exemplary SBS systems and methods which can be utilized with the methods and systems described herein are described in U.S. Patent Application Publication No. 2007/0166705, U.S. Patent Application Publication No. 2006/0188901, U.S. Pat. No. 7,057,026, U.S. Patent Application Publication No. 2006/0240439, U.S. Patent Application Publication No. 2006/0281109, PCT Publication No. WO 05/065814, U.S. Patent Application Publication No. 2005/0100900, PCT Publication No. WO 06/064199 and PCT Publication No. WO 07/010,251, the disclosures of which are incorporated herein by reference in their entireties and for all purposes.
Some embodiments can utilize sequencing by ligation techniques. Such techniques utilize DNA ligase to incorporate nucleotides and identify the incorporation of such nucleotides. Example ligation-based systems and methods which can be utilized with the methods and systems described herein are described in U.S. Pat. No. 6,969,488, U.S. Pat. No. 6,172,218, and U.S. Pat. No. 6,306,597, the disclosures of which are incorporated herein by reference in their entireties and for all purposes.
Some embodiments can utilize nanopore sequencing (Deamer, D. W. & Akeson, M. “Nanopores and nucleic acids: prospects for ultrarapid sequencing.” Trends Biotechnol. 18:147-151 (2000); Deamer, D. and D. Branton, “Characterization of nucleic acids by nanopore analysis”. Acc. Chem. Res. 35:817-825 (2002); Li, J., M. Gershow, D. Stein, E. Brandin, and J. A. Golovchenko, “DNA molecules and configurations in a solid-state nanopore microscope” Nat. Mater. 2:611-615 (2003), the disclosures of which are incorporated herein by reference in their entireties and for all purposes). In such embodiments, the target nucleic acid or nucleotides released from the target nucleic acid pass through a nanopore. The nanopore can be a synthetic pore or biological membrane protein, such as .alpha.-hemolysin. As the target nucleic acid or nucleotides pass through the nanopore, each base-pair (or base) can be identified by measuring fluctuations in the electrical conductance of the pore. (U.S. Pat. No. 7,001,792; Soni, G. V. & Meller, “A. Progress toward ultrafast DNA sequencing using solid-state nanopores.” Clin. Chem. 53:1996-2001 (2007); Healy, K. “Nanopore-based single-molecule DNA analysis.” Nanomed. 2:459-481 (2007); Cockroft, S. L., Chu, J., Amorin, M. & Ghadiri, M. R. “A single-molecule nanopore device detects DNA polymerase activity with single-nucleotide resolution.” J. Am. Chem. Soc. 130:818-820 (2008), the disclosures of which are incorporated herein by reference in their entireties and for all purposes).
Some embodiments can utilize methods involving the real-time monitoring of DNA polymerase activity. Nucleotide incorporations can be detected through fluorescence resonance energy transfer (FRET) interactions between a fluorophore-bearing polymerase and .gamma.-phosphate-labeled nucleotides as described, for example, in U.S. Pat. No. 7,329,492 and U.S. Pat. No. 7,211,414 (each of which is incorporated herein by reference in their entireties and for all purposes) or nucleotide incorporations can be detected with zero-mode waveguides as described, for example, in U.S. Pat. No. 7,315,019 (which is incorporated herein by reference in its entirety and for all purposes) and using fluorescent nucleotide analogs and engineered polymerases as described, for example, in U.S. Pat. No. 7,405,281 and U.S. Patent Application Publication No. 2008/0108082 (each of which is incorporated herein by reference in their entireties and for all purposes). The illumination can be restricted to a zeptoliter-scale volume around a surface-tethered polymerase such that incorporation of fluorescently labeled nucleotides can be observed with low background (Levene, M. J. et al. “Zero-mode waveguides for single-molecule analysis at high concentrations.” Science 299:682-686 (2003); Lundquist, P. M. et al. “Parallel confocal detection of single molecules in real time.” Opt. Lett. 33:1026-1028 (2008); Korlach, J. et al. “Selective aluminum passivation for targeted immobilization of single DNA polymerase molecules in zero-mode waveguide nanostructures.” Proc. Natl. Acad. Sci. USA 105:1176-1181 (2008), the disclosures of which are incorporated herein by reference in their entireties and for all purposes). In one example single molecule, real-time (SMRT) DNA sequencing technology provided by Pacific Biosciences Inc. can be utilized with the methods described herein. In some embodiments, a SMRT chip or the like may be utilized (U.S. Pat. Nos. 7,181,122, 7,302,146, 7,313,308, incorporated by reference in their entireties and for all purposes). A SMRT chip comprises a plurality of zero-mode waveguides (ZMW). Each ZMW comprises a cylindrical hole tens of nanometers in diameter perforating a thin metal film supported by a transparent substrate. When the ZMW is illuminated through the transparent substrate, attenuated light may penetrate the lower 20-30 nm of each ZMW creating a detection volume of about 1.times.10-21 L. Smaller detection volumes increase the sensitivity of detecting fluorescent signals by reducing the amount of background that can be observed.
An additional example of a sequencing platform that may be used in association with some of the embodiments described herein is provided by Helicos Biosciences Corp. In some embodiments, TRUE SINGLE MOLECULE SEQUENCING (tSMS)™. can be utilized (Harris T. D. et al., “Single Molecule DNA Sequencing of a viral Genome” Science 320:106-109 (2008), incorporated by reference in its entirety and for all purposes). In one embodiment, a library of target nucleic acids can be prepared by the addition of a 3′ poly(A) tail to each target nucleic acid. The poly(A) tail hybridizes to poly(T) oligonucleotides anchored on a glass cover slip. The poly(T) oligonucleotide can be used as a primer for the extension of a polynucleotide complementary to the target nucleic acid. In one embodiment, fluorescently-labeled nucleotide monomer, namely, A, C, G, or T, are delivered one at a time to the target nucleic acid in the presence DNA polymerase. Incorporation of a labeled nucleotide into the polynucleotide complementary to the target nucleic acid is detected, and the position of the fluorescent signal on the glass cover slip indicates the molecule that has been extended. The fluorescent label is removed before the next nucleotide is added to continue the sequencing cycle. Tracking nucleotide incorporation in each polynucleotide strand can provide sequence information for each individual target nucleic acid.
An additional example of a sequencing platform that can be used in association with the methods described herein is provided by Complete Genomics Inc. Libraries of target nucleic acids can be prepared where target nucleic acid sequences are interspersed approximately every 20 by with adaptor sequences. The target nucleic acids can be amplified using rolling circle replication, and the amplified target nucleic acids can be used to prepare an array of target nucleic acids. Methods of sequencing such arrays include sequencing by ligation, in particular, sequencing by combinatorial probe-anchor ligation (cPAL).
In some embodiments using cPAL, about 10 contiguous bases adjacent to an adaptor may be determined. A pool of probes that includes four distinct labels for each base (A, C, T, G) is used to read the positions adjacent to each adaptor. A separate pool is used to read each position. A pool of probes and an anchor specific to a particular adaptor is delivered to the target nucleic acid in the presence of ligase. The anchor hybridizes to the adaptor, and a probe hybridizes to the target nucleic acid adjacent to the adaptor. The anchor and probe are ligated to one another. The hybridization is detected and the anchor-probe complex is removed. A different anchor and pool of probes is delivered to the target nucleic acid in the presence of ligase.
The sequencing methods described herein can be advantageously carried out in multiplex formats such that multiple different target nucleic acids are manipulated simultaneously. In particular embodiments, different target nucleic acids can be treated in a common reaction vessel or on a surface of a particular substrate. This allows convenient delivery of sequencing reagents, removal of unreacted reagents and detection of incorporation events in a multiplex manner. In embodiments using surface-bound target nucleic acids, the target nucleic acids can be in an array format. In an array format, the target nucleic acids can be typically bound to a surface in a spatially distinguishable manner. The target nucleic acids can be bound by direct covalent attachment, attachment to a bead or other particle or binding to a polymerase or other molecule that is attached to the surface. The array can include a single copy of a target nucleic acid at each site (also referred to as a feature) or multiple copies having the same sequence can be present at each site or feature. Multiple copies can be produced by amplification methods such as, bridge amplification or emulsion PCR as described in further detail herein.
Methods for amplification of nucleic acids are well known in the art. Any appropriate method of amplification may be used in conjunction with the methods disclosed herein. For example, a useful amplification technique is PCR (polymerase chain reaction). Methods of PCR include basic PCR (Saiki et al., Science 1985, 230:1350-1354), real-time PCR (RT-PCR) (Nanashima et al., J. Biol. Chem. 2008, 283:16868-16875), hot-start PCR (Carothers et al., Biotechniques 1989, 7:494-9 1989; Krishnan et al. Nucl. Acids Res. 1991, 19:1153; Clark, Nucl. Acids Res. 1988, 16:9677-86; Lin & Jayasena, J. Mol. Biol. 1997, 271:100-11; Dang & Jayasena, J. Mol. Biol. 1996, 264:268-78; Scalice et al. J. Immunol. Methods, 1994, 172:147-63; Sharkey et al., Biotechnology 1994, 12:506-9; Moretti, T. et al., BioTechniques 1998, 25:716-22), long PCR (Barnes, Proc. Natl. Acad. Sci. USA 1994, 91:2216-20), quantitative endpoint PCR (Gaudette & Crain, Nucl. Acids Res. 1991, 19:1879-84; Murphy et al., Biochemistry 1990, 29:10351-10356), quantitative real-time PCR (Lee et al., Nucl. Acids Res. 1993, 21:3761-3766; Bernard et al., Anal. Biochem. 1998, 255:101-107; Sherrill et al., J. Am. Chem. Soc. 2004, 126:4550-4556; Frackman et al., Promega Notes 2006, 92:10-13); rapid amplified polymorphic DNA analysis (McClelland & Welsh, PCR Methods Appl. 1994, 4:S59-65; Power, J. Hosp. Infect. 1996, 34:247-265; Black, 1993), rapid amplification of cDNA ends (Troutt et al., Proc. Natl. Acad. Sci. USA 1992, 89:9823-9825; Edwards et al., Methods in Molecular Biology (Vol. 15), White, B. A., ed., Humana Press, Totowa, N.J., 1991; Liu & Gorovsky, Nucl. Acids Res. 1993, 21:4954-60; Fromont-Racine et al., Nucl. Acids Res. 1993, 21:1683-1684), differential display PCR (Liang & Pardee, Science 1992, 257:967-71), in situ PCR (Haase et al., Proc. Natl. Acad. Sci. USA 1990, 87:4971-4975), and high fidelity PCR (Cline et al., Nucl. Acids Res. 1996, 24:3546-3551).
Other means of amplifying nucleic acid that can be used in the methods of the provided invention include, for example, reverse transcription-PCR, real-time PCR, quantitative real-time PCR, digital PCR (dPCR), digital emulsion PCR (dePCR), clonal PCR, amplified fragment length polymorphism PCR (AFLP PCR), allele specific PCR, assembly PCR, asymmetric PCR (in which a great excess of primers for a chosen strand is used), colony PCR, helicase-dependent amplification (HDA), Hot Start PCR, inverse PCR (IPCR), in situ PCR long PCR (extension of DNA greater than about 5 kilobases), multiplex PCR, nested PCR (uses more than one pair of primers), single-cell PCR, touchdown PCR, loop-mediated isothermal PCR (LAMP), and nucleic acid sequence based amplification (NASBA). Other amplification schemes include: Ligase Chain Reaction, Branch DNA Amplification, Rolling Circle Amplification. Circle to Circle Amplification, SPIA amplification, Target Amplification by Capture and Ligation (TACL) amplification, and RACE amplification.
Nucleic acid molecules can be amplified on beads, for example using emulsion PCR methods. Exemplary emulsion-based amplification techniques that can be used in a method disclosed herein are described in US 2005/0042648; US 2005/0079510; US 2005/0130173 and WO 05/010145, each of which is incorporated herein by reference in its entirety and for all purposes. As further described herein, nucleic acid molecules can be amplified on a surface using bridge amplification to form nucleic acid clusters. Exemplary methods of generating nucleic acid clusters for use in high-throughput nucleic acid technologies have been described. See, for example, U.S. Pat. No. 7,115,400, U.S. Patent Application Publication Nos. 2005/0100900 and 2005/0059048, and PCT Publication Nos. WO 98/44151, WO 00/18957, WO 02/46456, WO 06/064199, and WO 07/010,251, each of which is incorporated by reference herein in its entirety and for all purposes.
RNA EXTRACTION. The RNA may be obtained from a cell using techniques known in the art. Typically, the cell is lysed and the RNA is recovered using known nucleic acid purification techniques. Thus, a method set forth herein includes lysing the T cell, thereby providing the plurality of nucleic acids (e.g., RNA molecules).
aConv, Conventional peripheral blood stem cell graft; TCD, T-cell-depleted peripheral blood stem cell graft; DUCB, Double-unit umbilical cord blood graft; Healthy, Healthy donor.
b NHL, Non-Hodgkin's lymphoma; FL, follicular lymphoma; MZL, Marginal zone lymphoma; SLL, Small lymphocytic lymphoma; DLBCL, Diffuse large B-cell lymphoma; CLL, chronic lymphocytic leukemia; HL,
cCy, Cyclophosphamide; Flu, Fludarabine; TBI, Total body irradiation; Rtx, Rituximab; Mel, Melphalan; Thio, Thiotepa; Clo, Clofarabine; Bu, Busulfan.
dMRD, Matched related donor; MMUD, mismatched unrelated donor; MUD, Matched unrelated donor.
eTacro, Tacrolimus; MMF, Mycophenolate mofetil; Siro, Sirolimus; CSA, Cyclosporine-A.
fCells/1.
gBK, BK polyomavirus; HSV, Herpes simplex virus; RV, Rhinovirus; CMV, Cytomegalovirus; EBV, Epstein-Barr virus; RSV, Respiratory syncytial virus; FLU, Influenza virus; HHV6, Human Herpesvirus 6; RV, Rotavirus; MPV, Metapneumovirus.
h T-cell-depleted bone marrow graft.
iMild oral and eye symptoms only.
jMild eye symptoms only.
k Ongoing acute GVHD.
lActive steroids.
mAll patients with CMV reactivation were successfully treated for CMV viremia and did not progress to CMV disease.
nPatients had documented EBV viremia and post-transplant lymphoproliferative disease; and were treated with rituximab.
oPatient had documented EBV viremia, but no documented post-transplant lymphoproliferative disease; and was treated with rituximab.
pInfection within three months of transplantation. n/a, not applicable; lim, limited; ext, extensive.
aOn protocol 07-127 (IL-7 9/21-28 Oct. 15, 2010). Bcr/abl pcr+ Jan. 25, 11. DLI Sep. 28, 2011. Moderate cGVHD after DLL
b Dry eyes
0101/01N
The contents of each of the following is hereby incorporated by reference as if fully set forth herein, except for terminology that is inconsistent with the terminology used herein.
This application claims priority to U.S. Provisional Application Ser. No. 61/667,783 filed on Jul. 3, 2012 the entire contents of which are hereby incorporated by reference as if fully set forth herein, under 35 U.S.C. §119(e).
This invention was made with Government support under Contract No. HL069929, CA107096 and A1080455 awarded by the National Institutes of Health (NIH) and under Contract No. W81XWH-09-1-0294 awarded by US Department of Defense. The Government has certain rights in the invention.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2013/049404 | 7/3/2013 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61667783 | Jul 2012 | US |
