Patent Application
20140075585
The present invention relates to CD82 polypeptides of the mammalian tetraspanin CD82 protein family for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection. The present invention furthermore relates to CD82 knockout and transgenic animals and their cells, tissues and organs. The present invention furthermore relates to antibodies against a CD82 polypeptide, pharmaceutical compositions comprising at least one inhibitor of a CD82 polypeptide or comprising cells, tissues and organs of animals in which the CD82 level, expression and/or activity is modified, and their use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection. The present invention furthermore relates to methods of diagnosing xenograft recognition and/or rejection and methods for the prevention and/or treatment of xenograft recognition and/or rejection as well as methods of xenotransplantation.
After all pharmacological interventions have failed, there exists a growing number of patients requiring immediate alternatives to human organ donations; since the number of available donor organs cannot keep up with the demand for such organs. Tragically, the acute shortage of donor organs leads to so many deaths of patients in dire need of transplantation. The number of heart transplants fluctuates around the 3,700 mark as reported by the registry of the International Society for Heart and Lung Transplantation [1]. It is estimated that the number of patients requiring transplantation is around 800,000 while the total number of heart transplantation in 2007 reached a maximum of only 3,500 transplants [2].
One viable option for overcoming the donor organ shortage is the use of animal organs as replacement i.e. “xenotransplantation”. Initially, a transplanted organ between discordant species appears viable and healthy, but this is rapidly followed by an acute irreversible rejection: the hyperacute rejection (HAR). HAR is attributed to xenoreactive natural antibodies (XNA) and complement activation [3-6]. XNA target galactose α1,3-galactose (Galα1,3-gal) structures that decorate proteins and lipids of the transplanted organ endothelium [7]. These “decorations” are brought about by the enzyme alpha 1,3-galactosyltransferase which is expressed in all mammals except human, apes and old world monkeys [8-10]. Many strategies have been employed in order to overcome HAR. These include, removal of the anti-Galα1,3-gal antibodies, accommodation, transgenesis and siRNA silencing of the alpha 1,3 galactosyl transferase. Transgenesis gave a glimpse of hope through extending the life of the transplanted organ which, however, eventually succumbed to rejection albeit at a considerably later time [11, 12]. Clinical xenotransplantation is controversial due to the identified rejection problems and the possibility of xenozoonotic diseases [10].
Previously, the inventors have identified innate immune cells as an independent player in the xenograft rejection in the absence of xenoreative natural antibodies and complement [13-15]. The inventors demonstrated that human naive neutrophils are capable of recognizing and activating porcine naive endothelial cells through a calcium dependent mechanism independently of XNA and complement and under conditions in which all binding sites for α-gal epitope are blocked by saturating concentrations of anti-α-gal antibodies [16, 17]. Similar results were obtained for other innate immune cells; namely NK cells under static and flow conditions [13]. The molecular mechanism(s) underlying such recognition have yet to be determined.
There is a need for means and methods for the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
According to the present invention this object is solved by a CD82 polypeptide of the mammalian tetraspanin CD82 protein family for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
According to the present invention this object is solved by an antibody against a CD82 polypeptide.
According to the present invention this object is solved by a knockout non-human mammal whose genome comprises a homozygous or heterozygous disruption in a gene encoding a CD82 polypeptide of the mammalian tetraspanin CD82 protein family.
According to the present invention this object is solved by a transgenic, non-human mammal, wherein the cells of said non-human mammal fail to express a functional CD82 polypeptide of the mammalian tetraspanin CD82 protein family or wherein the cells of said non-human mammal comprise a coding region of a CD82 polypeptide of the mammalian tetraspanin CD82 protein family under the control of a heterologous promoter active in the cells of said non-human mammal.
According to the present invention this object is solved by a cell, a tissue or an organ obtained from a knockout or transgenic mammal of the invention.
According to the present invention this object is solved by providing said cell(s), tissue(s) and/or organ(s) for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
According to the present invention this object is solved by providing said cell(s), tissue(s) and/or organ(s) for use in xenotransplantation, for example, as xenografts.
According to the present invention this object is solved by a pharmaceutical composition comprising at least one inhibitor of a CD82 polypeptide, optionally, a pharmaceutical excipient, and optionally, a pharmaceutical carrier.
According to the present invention this object is solved by a pharmaceutical composition comprising cell(s), tissue(s) and/or organ(s) obtained from an animal in which the CD82 level, expression and/or activity is modified or inhibited, optionally, a pharmaceutical excipient, and optionally, a pharmaceutical carrier.
According to the present invention this object is solved by the antibody or the pharmaceutical composition according to the invention for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
According to the present invention this object is solved by a method for the diagnosis of xenograft recognition and/or rejection comprising determining CD82 expression levels in patient specimen.
According to the present invention this object is solved by a method for the prevention and/or treatment of xenograft recognition and/or rejection, comprising the step of administering to a patient an effective amount of at least one inhibitor of a CD82 polypeptide of the mammalian tetraspanin CD82 protein family; and/or administering to a patient cell(s), tissue(s) and/or organ(s) obtained from an animal in which the CD82 level, expression and/or activity is modified or inhibited.
According to the present invention this object is solved by a method of xenotransplantation, comprising the step of administering to a patient cell(s), tissue(s) and/or organ(s) obtained from a donor animal in which the CD82 level, expression and/or activity is modified or inhibited.
Before the present invention is described in more detail below, it is to be understood that this invention is not limited to the particular methodology, protocols and reagents described herein as these may vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention which will be limited only by the appended claims. Unless defined otherwise, all technical and scientific terms used herein have the same meanings as commonly understood by one of ordinary skill in the art. For the purpose of the present invention, all references cited herein are incorporated by reference in their entireties.
As described above, the present invention provides a CD82 polypeptide of the mammalian tetraspanin CD82 protein family for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
The present invention provides the use of a CD82 polypeptide of the mammalian tetraspanin CD82 protein family for the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
As used herein, the term “xenotransplantation” refers the transplantation of living cells, tissues or organs from one species to another. Such cells, tissues or organs are called “xenografts” or “xenotransplants”. As used herein, the term “xenotransplantation” preferably refers to the transplantation of animal living cells, tissues or organs to a patient, i.e. a human recipient.
To date no xenotransplantation trials have been entirely successful due to the many obstacles arising from the response of the recipient's immune system. This response, which is generally more extreme than in allotransplantations, ultimately results in rejection of the xenograft, and can in some cases result in the immediate death of the recipient. There are several types of rejection of xenografts, these include: hyperacute rejection (HAR), acute vascular rejection, cellular rejection, chronic rejection.
As used herein, the term “xenograft recognition and/or rejection” refers to all mechanisms of the recipient after xenotransplantation, including the above.
CD82, also known as C33 antigen or KAI1 originally identified as a marker for “activation/differentiation” of mononuclear cells [25], is a member of the tetraspanin family of proteins responsible for divergent cellular activities including activation, differentiation, motility, adhesion, signaling, fusion and metastasis. They are highly conserved and can be found in species as disparate as fungi and mammals. In human, CD82 is expressed in many cell types including lymphocytes, granulocytes, epithelial cells, platelets, endothelial cells and fibroblasts. Thirty four (34) mammalian tetraspanins were identified with thirty three (33) expressed in human [26]. All have four transmembrane domains with cytosolic N- and C-terminal regions and two extracellular domains with conserved CCG motif [26-28]. CD82 exists as two isoforms resulting from two distinct splice variants. CD82 is heavily palmitoylated and glycated [29, 30] and together with other proteins, constitutes the tetraspanin web. The web is a complex entity invoking functional diversity in stimulus response coupling [see e.g. Lazo P A, http://atlasgeneticsoncology.org//Deep/TetraspaninID20062.html.].
The amino acid sequence of SEQ ID NO. 1 shows the human CD82 splice variant V1 (Genebank Accession No. NM—002231) (isoform 1); and the amino acid sequence of SEQ ID NO. 2 shows the human CD82 splice variant V2 (Genebank Accession No. NM—001024844) (isoform 2).
In a preferred embodiment, the CD82 polypeptide comprises the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
In one embodiment, the CD82 polypeptide consists of the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2.
Preferably the CD82 polypeptide is encoded by a nucleotide sequence encoding the amino acid sequence of SEQ ID NO. 1 or of SEQ ID NO. 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
In a preferred embodiment, the diagnosis of said xenograft recognition and/or rejection comprises determining CD82 expression levels in patient specimen and/or specimen of the xenograft recipient. This expression levels may be determined by mRNA levels and protein levels in cells, tissues, organs and sera and other bodily fluids.
In a preferred embodiment, the prevention and/or treatment of said xenograft recognition and/or rejection comprises modulating CD82 expression and/or activity, preferably inhibiting CD82 expression and/or activity.
The CD82 expression and/or activity can be modulated, preferably inhibited, in the donor of the xenograft (such as a pig or sheep) and/or in the recipient of the xenograft (such as a patient, a human recipient).
Preferably, an inhibitor of the CD82 polypeptide is utilized for said inhibition of CD82 expression and/or activity.
Preferably, the inhibitor is
(i) an anti-CD82 antibody,
(ii) small molecule inhibitor(s) of the CD82 expression and/or activity.
In a preferred embodiment, the anti-CD82 antibody is an antibody according to the present invention, as described herein.
Preferably, an antibody according to the present invention is an antibody against:
or
or
or
Preferably, small molecule inhibitor(s) of the CD82 expression and/or activity are siRNA(s), antisense oligonucleotide(s), transcription and/or translation inhibitor(s), activity inhibitors or modulators.
Preferably, the inhibitor is administered to a subject in need thereof.
The administration can be by inhalation, intranasal, intravenous, oral, transdermal, sustained release, controlled release, delayed release, suppository, or sublingual administration.
In one embodiment, the inhibitor is administered to a subject in need thereof in combination with at least one immunosuppressive agent.
Preferably, the immunosuppressive agent is selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
CD82 Knockout and Transgenic Animals and their Cells, Tissues and Organs
As described above, the present invention provides CD82 knockout animals and CD82 transgenic animals.
A CD82 knockout animal according to the invention is preferably a knockout non-human mammal whose genome comprises a homozygous or heterozygous disruption in a gene encoding a CD82 polypeptide of the mammalian tetraspanin CD82 protein family.
The CD82 transgenic animals of the invention are animals in which the CD82 level, expression and/or activity is modified or inhibited.
A CD82 transgenic animal according to the invention is preferably a transgenic, non-human mammal, wherein the cells of said non-human mammal fail to express a functional CD82 polypeptide of the mammalian tetraspanin CD82 protein family or wherein the cells of said non-human mammal comprise a coding region of a CD82 polypeptide of the mammalian tetraspanin CD82 protein family under the control of a heterologous promoter active in the cells of said non-human mammal.
The knockout or transgenic mammal of the invention is preferably a pig or a sheep.
The CD82 of a knockout or transgenic mammal of the invention preferably refers to a CD82 polypeptide which comprises the amino acid sequence of SEQ ID NO. 1 or 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at, least 95% or at least 99% identity; and/or to a CD82 polypeptide which is encoded by a nucleotide sequence encoding the amino acid sequence of SEQ ID NO. 1 or 2 or encoding an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
In one embodiment, the CD82 of a knockout or transgenic mammal of the invention refers to a CD82 polypeptide which consists of the amino acid sequence of SEQ ID NO. 1 or of SEQ ID NO. 2.
Preferably, the CD82 knockout animals and/or the CD82 transgenic animals are used as the donor animals for xenotransplantation, i.e. as the donor animals of a xenograft.
As described above, the present invention provides cell(s), tissue(s) and/or organ(s) obtained from the CD82 knockout or transgenic mammal(s) of the invention.
As described above, the present invention provides the cell(s), tissue(s) and/or organ(s) obtained from the CD82 knockout or transgenic mammal(s) of the invention for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
As described above, the present invention also provides the cell(s), tissue(s) and/or organ(s) obtained from the CD82 knockout or transgenic mammal(s) of the invention for use in xenotransplantation, i.e. as xenografts.
Said use comprises the administration of the cell(s), tissue(s) and/or organ(s) of the invention to a subject in need thereof.
Antibodies and Pharmaceutical Compositions and their Uses
As described above, the present invention provides an antibody against a CD82 polypeptide.
Preferably, an antibody according to the present invention is an antibody against:
or
or
or
As described above, the present invention provides pharmaceutical compositions.
In one embodiment, the pharmaceutical composition comprises
at least one inhibitor of a CD82 polypeptide,
optionally, a pharmaceutical excipient, and
optionally, a pharmaceutical carrier.
In a preferred embodiment of the above pharmaceutical composition, the at least one inhibitor is
In a preferred embodiment of the above pharmaceutical composition, the animal in which the CD82 level, expression and/or activity is modified or inhibited and from which the cell(s), tissue(s) and/or organ(s) are obtained from, is an CD82 knockout or transgenic mammal of the invention.
In a preferred embodiment of the above pharmaceutical composition, the cell(s), tissue(s) and/or organ(s) are the cell(s), tissue(s) and/or organ(s) obtained from the CD82 knockout or transgenic mammal(s) of the invention.
In one embodiment, the carrier, if present, is aqueous.
In one embodiment, a pharmaceutical composition of the present invention furthermore comprises at least one immunosuppressive agent.
The immunosuppressive agent is preferably selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
As described above, the present invention provides the antibody according to the present invention or the pharmaceutical composition according to the present invention for use in the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
As described above, the present invention provides the use of an antibody according to the present invention or the use of a pharmaceutical composition according to the present invention for the diagnosis, prevention and/or treatment of xenograft recognition and/or rejection.
Preferably, the antibody or the pharmaceutical composition is administered to a subject in need thereof.
The administration can be by inhalation, intranasal, intravenous, oral, transdermal, sustained release, controlled release, delayed release, suppository, or sublingual administration.
In one embodiment, the antibody or the pharmaceutical composition is administered to a subject in need thereof in combination with at least one immunosuppressive agent.
The immunosuppressive agent is preferably selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
As described above, the present invention provides a method for the diagnosis of xenograft recognition and/or rejection.
Said method comprises determining CD82 expression levels in patient specimen.
The patient specimen are preferably specimen of the xenograft recipient, such as blood, serum, urine, tissue samples, cells or organs.
Methods for Preventing and/or Treating Xenograft Recognition and/or Rejection
As described above, the present invention provides method(s) for the prevention and/or treatment of xenograft recognition and/or rejection.
Said method for the prevention and/or treatment of xenograft recognition and/or rejection, comprises the step of
administering to a patient an effective amount of at least one inhibitor of a CD82 polypeptide of the mammalian tetraspanin CD82 protein family;
and/or
administering to a patient cell(s), tissue(s) and/or organ(s) obtained from an animal in which the CD82 level, expression and/or activity is modified or inhibited.
In one embodiment, the present invention provides method(s) for the prevention and/or treatment of xenograft recognition and/or rejection through methods of xenotransplantation of a CD82-modified xenograft.
As described herein, the CD82 polypeptide preferably comprises the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
As described herein, in one embodiment the CD82 polypeptide consists of the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2.
As described herein, the CD82 polypeptide is preferably encoded by a nucleotide sequence encoding the amino acid sequence of SEQ ID NO. 1 or 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
As described herein, said inhibitor is preferably
(i) an anti-CD82 antibody,
(ii) small molecule inhibitor(s) of the CD82 expression and/or activity,
The administration can be by inhalation, intranasal, intravenous, oral, transdermal, sustained release, controlled release, delayed release, suppository, or sublingual administration.
As described herein, in one embodiment, the inhibitor is administered to the patient in combination with at least one immunosuppressive agent.
The immunosuppressive agent is preferably selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
As described herein, said animal in which the CD82 level, expression and/or activity is modified or inhibited is preferably a CD82 knockout animal or a CD82 transgenic animal according to the invention.
As described herein, said cell(s), tissue(s) and/or organ(s) are the cell(s), tissue(s) and/or organ(s) are preferably obtained from the CD82 knockout animal or a CD82 transgenic animal according to the invention.
As described herein, the cell(s), tissue(s) and/or organ(s) are preferably administered to the patient.
The administration can be by inhalation, intranasal, intravenous, oral, transdermal, sustained release, controlled release, delayed release, suppository, or sublingual administration.
As described herein, in one embodiment, the cell(s), tissue(s) and/or organ(s) are administered to the patient in combination with at least one immunosuppressive agent.
The immunosuppressive agent is preferably selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
In one embodiment, administration of the at least one inhibitor is carried out together with an administration of the cell(s), tissue(s) and/or organ(s).
As described above, the present invention provides method(s) of xenotransplantation.
Said method of xenotransplantation comprises the step of
administering to a patient cell(s), tissue(s) and/or organ(s) obtained from a donor animal in which the CD82 level, expression and/or activity is modified or inhibited.
As described herein, the CD82 polypeptide preferably comprises the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
As described herein, in one embodiment the CD82 polypeptide consists of the amino acid sequence of SEQ ID NO. 1 or SEQ ID NO. 2.
As described herein, the CD82 polypeptide is preferably encoded by a nucleotide sequence encoding the amino acid sequence of SEQ ID NO. 1 or 2 or an amino acid sequence having at least 80% sequence identity to SEQ ID NO. 1 or 2, preferably at least 90%, more preferably at least 95% or at least 99% identity.
As described herein, said animal in which the CD82 level, expression and/or activity is modified or inhibited is preferably a CD82 knockout animal or a CD82 transgenic animal according to the invention.
As described herein, said cell(s), tissue(s) and/or organ(s) are the cell(s), tissue(s) and/or organ(s) are preferably obtained from the CD82 knockout animal or a CD82 transgenic animal according to the invention.
The cell(s), tissue(s) and/or organ(s) of the CD82 knockout animal or a CD82 transgenic animals of the invention are utilized as the xenografts.
As described herein, the cell(s), tissue(s) and/or organ(s) are preferably administered to the patient.
As described herein, in one embodiment, the cell(s), tissue(s) and/or organ(s) are administered to the patient in combination with at least one immunosuppressive agent.
The immunosuppressive agent is preferably selected from azathioprene, cyclosporine, glucocorticoid and pharmaceutically acceptable salts thereof.
Here we used porcine endothelial cells from wild type and α-gal-knockout animals to demonstrate that recognition of xenogeniec endothelial cells occurs independently of α-gal structures. We used three human derived pro-myeloid cell lines; HL60, THP-1 and KG-1 which, in their undifferentiated state do not recognize xenogeneic endothelial cells as defined by the lack of calcium transients and ROM production in response to POAECs; however, after differentiation, these cells transiently raise their intracellular calcium and increase ROM production upon exposure to POAECs. In order to identify possible α-gal-independent site(s) mediating recognition of xenogeneic endothelial cells, we used Serial Analysis of Gene Expression (SAGE) of the promyelocytic cell lines together with that of human naive neutrophils. We created SAGE libraries of these cell lines and use them to identify SAGE transcripts before and after differentiation, and compared those to SAGE transcripts in resting human naive neutrophils. SAGE libraries of these cell lines were used to compare transcriptional activities before and after differentiation with that of human naive neutrophils. This strategy yielded a number of transcripts that were: (1) differentially expressed in all of the differentiated vs undifferentiated cell lines; (2) constitutively expressed in human naive neutrophils. Twelve differentially expressed transcripts were identified by this approach with only six (6) displaying consistent change in all cell lines. Since our putative xeno-recognition moiety(s) should be (1) trans plasma membrane protein(s) and (2) associated with intracellular calcium release, only one out of the six identified transcripts, belonging to the tetraspanin CD82, satisfied the above criteria and was therefore considered the likely candidate mediating the recognition of xeno-endothelial cells independently of Galα-1,3-gal. his was confirmed by our finding that blocking antibodies to CD82 inhibited both the calcium rise and ROM production in human naïve neutrophils upon exposure to POAECs. Thus, it appears that CD82 mediated recognition is the mechanism used by innate immune cells to identify xenogeneic endothelial cells and thus responsible for delayed xenograft rejection.
Alpha-gal 1,3 gal was identified as the major barrier to xenotransplantation of animal organs into non-human primates. Hyperacute rejection of transplanted xenogeneic organs was attributed to xenoreactive natural antibodies against Galα-1,3-gal decorated proteins and lipids on the xenograft and complement activation, leading to the demise of transplanted vascularized xenograft within minutes [3-6]. Organs from Galα-1,3-gal knock out animals were also rejected albeit after a relatively prolonged survival with immunosupression [11]. The fact however, remains that the necessary sustained survival of transplanted xenografts is yet to be achieved, prompting a serious search for putative mechanism(s) involved in the eventual rejection of the transplanted xenograft. In addition, human naïve innate immune cells recognize, activate and are activated by xenogeneic endothelial cells in the absence of xenoreactive natural antibodies and complement, and under conditions in which all alpha-gal binding sites were blocked by anti-gal IgG [13, 15-17].
In the present work we demonstrate that human naive neutrophils are activated by xenogeneic porcine aortic endothelial cells but not by allogeneic human aortic endothelial cells or HUVECs. This suggests that the recognition of xenogeneic endothelial cells by human naïve neutrophils occurs in an Galα-1,3-gal-independent manner. To identify the molecular moiety(s) involved in this recognition we used progranulocytic cell lines which in their undifferentiated state are not activated by xenogeneic endothelial cells, and only become activated after differentiation into neutrophil-like or monocyte-like cells. SAGE analysis of these cells and of resting human naïve neutrophils revealed six different transcripts that were consistently over expressed in the differentiated cell lines and thus are the likely candidates' transcripts responsible for xenorecognition and subsequent activation of these cell lines by xenogeneic endothelial cells. Out of these six, only CD82 was identified as an integral plasma membrane protein, suggesting that CD82 was the likely candidate responsible for xenoendothelial cell recognition. Three lines of evidence support such a claim:
(1) Undifferentiated cell lines HL-60, KG-1 and THP-1 expressing relatively low levels of CD 82 at both the message and protein levels do not evoke a calcium transient or ROM production in response to POAECs.
(2). Differentiated HL-60, KG-1 and THP-1 and human naïve neutrophils expressing relatively higher levels of CD82 do respond to xenogeneic POAECs.
(3) Antibodies to CD82 can inhibit both calcium transient and ROM production in response to xenogeneic insult.
CD82 also known as C33 antigen or KAI1 originally identified as a marker for “activation/differentiation” of mononuclear cells [25], is a member of the tetraspanin family of proteins responsible for divergent cellular activities including activation, differentiation, motility, adhesion, signaling, fusion and metastasis. They are highly conserved and can be found in species as disparate as fungi and mammals. In human, CD82 is expressed in many cell types including lymphocytes, granulocytes, epithelial cells, platelets, endothelial cells and fibroblasts. Thirty four (34) mammalian tetraspanins were identified with thirty three (33) expressed in human [26]. All have four transmembrane domains with cytosolic N- and C-terminal regions and two extracellular domains with conserved CCG motif [26-28]. CD82 exists as two isoforms resulting from two distinct splice variants. CD82 is heavily palmitoylated and glycated [29, 30] and together with other proteins, constitutes the tetraspanin web. The web is a complex entity invoking functional diversity in stimulus response coupling [see e.g. Lazo P A, http://atlasgeneticsoncology.org//Deep/TetraspaninlD20062. html.]. Furthermore, CD82 was demonstrated to link lipid rafts to the actin cytoskeleton and depletion of cholesterol seems to inhibit CD82 dependent responses. Tetraspanins have long been considered as membrane organizers [31, 32] and are known to interact with a number of integrins, growth factors, lipid rafts, actin cytoskeleton and membrane domains; suggesting their involvement in immune responses and immune synapse [33]. Immune synapse is a major intercellular contact milieu where different proteins cluster to assemble to perform a variety of functions.
Loss of CD82 expression has been correlated with increase metastasis in colorectal cancers, squamous cell carcinoma, prostate cancer, breast cancer, and hepatocellular carcinoma [e.g. 34, 35]. However, its role in primary tumor growth is not well defined [36]. Tumor metastasis suppression by CD82 is mediated through a number of molecular mechanisms including stablizing E-cadherin/beta-catenin complex formation, upregulation of Sprouty2, maturation of β-1 integrin and direct interactions with DARC-expressing endothelial cells with the subsequent inhibition of tumor cell proliferation and induction of senescence [37-40]. CD82 has been associated with suppression of tumor metastasis and this fact must be reconciled when designing strategies to reduce the CD82 levels in transplanted xenografts.
In conclusion CD82 is a valuable molecular moiety for developing targeted diagnostics and therapeutic modalities in order to extend the life of a transplanted xenograft and provide a viable alternative to the chronic shortage of suitable human organs.
The following examples and drawings illustrate the present invention without, however, limiting the same thereto.
(A) Confocal fluorescence micrographs showing the expression of alpha-gal in wild type (WT) and knockout (KO) POAECs (top left), and corresponding flowcytometric histograms from WT and KO POAECs (bottom left). The message level for alpha gal transferase is shown on the top right as ratio to the house keeping protein GAPDH in WT and KO POAECs.
(B) Calcium changes in human neutrophils at the indicated time intervals in seconds (s) invoked by exposure to alpha gal KO POAEC (top). Calcium changes are coded such that high calcium is indicated by white. Absolute calcium levels invoked in neutrophils by alpha gal KO POAECs (bottom).
(C) Calcium changes in human neutrophils invoked by WT POAECs (top left) and in the presence of saturating concentrations of antibodies to the alpha-gal (top right). Bottom graphs of (C) indicate the corresponding absolute calcium levels.
Reactive oxygen metabolite (ROM) production as measured by LDCL in human naive neutrophils after stimulation with POAECs (WT) and knockout POAECs (KO) and the lack of effect on HAECs.
NBT micrographs of undifferentiated and differentiated cell line. Differentiation is indicated by the reduction of soluble NBT to blue-black insoluble formazan (upper panel). Calcium homeostasis in undifferentiated and differentiated cell lines; KG1, HL60 and THP-1 (lower panel). First arrow indicates the time of addition of POAECs and second arrow indicates the time of addition of ionomycin 2 μM.
(A) Venn diagram of the differentially expressed genes in the three cell lines upon differentiation showing a common 12 genes that are consistently and differentially expressed. The heat map identifies the differentially expressed genes and their relative expression values as indicated by the bar.
(B) List of the differentially expressed genes in the KG-1, THP-1, HL60 cell lines expressed as fold increase and in human naive neutrophils expressed as counts.
(A) Expression of CD82 in differentiated and undifferentiated cell lines at the mRNA levels as indicated by ratio relative to the house keeping gene GAPDH levels.
(B) expression of CD82 at the protein levels where N is neutrophils, HU, TU and KU are undifferentiated and HD, TD and KD are differentiated HL60, THP-1 and KG-1 respectively.
(C) Confocal micrographs of human naive neutrophils in live cells immunostained for CD82.
Inhibition of calcium dependent recognition of POAECs by human neutrophils (upper panel). The lower graphs show absolute calcium levels in human neutrophils after exposure to POAECs in the presence (squares, i.e. lower line) and absence (diamonds, i.e. upper line) of blocking antibodies to CD82 (lower left). Inhibition of ROM production as indicated by LDCL is shown in lower right in the presence (lower line) and absence (upper line) of blocking antibodies to CD82.
Fluo-3 AM (4-(6-Acetoxymethoxy-2,7-dichloro-3-oxo-9-xanthenyl)-4′-methyl-2,2′-(ethylenedioxy)dianiline-N,N,N′,N′-tetraacetic acid tetrakis (acetoxymethyl) ester) was purchased from Molecular Probes (Invitrogen, Carlsbad, Calif.). LightCycler Instrument (Roche Diagnostics, Mannheim, Germany), LightCycler—DNA Master SYBR Green 1 was purchased from Roche Diagnostics (Mannheim, Germany). I-SAGE/1-Long SAGE kit with magnetic stand, Platinum TaqDNA polymerase, and Triazol solution were purchased from (Invitrogen, Carlsbad, Calif.). Cell lines were purchased from ATCC (ATCC, Rockville, Md.). Culture media; RPMI-1640 and DMEM were purchased from (Gibco BRL, Grand Island, N.Y.). All other reagent were Analar grade and were purchased from Sigma (MO, USA) and BDH Chemicals (UK). Fluo-3 AM, and 5-Amino-2,3-dihydro-1,4-phthalazinedione (luminol) were dissolved in dimethylsulfoxide (DMSO) and delivered to the cells at a final concentration of 1 μM, 11 μM, respectively; in a final DMSO concentration of 0.1%. Antibodies to von Willebrand Factor were purchased from (F3520; Sigma, Mo.); acetylated low-density lipoprotein (DiI-Ac-LDL; Biogenesis, Bournmouth UK); mouse anti human CD82 were purchsed from (Abeam and Santa Cruze, Calif., USA), anti-LFA-1α were purchased from R&D System (Mineapolis, USA). Secondary goat anti mouse FITC labeled were purchased from Santa Cruze (CA, USA) and Alexa 647 labeled were from Pierce (USA). PMA and Dimethylsulphoxide (DMSO), Bt2-cAMP, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT), Cell culture reagents, protease inhibitors, and other analytical grade reagents were purchased from Sigma-Aldrich (St Louis, Mo.). Restriction enzymes, NlaIII, MmeI, and Sph were purchased from New England Biolabs Inc., (Beverly, Mass.).
Porcine aortic endothelial cells (POAECs; P304K-05) and human aortic endothelial cells (HOAECs; 304K-05a) were purchased from Cell Application, Inc. (San Diego, Calif., USA). Human umbilical vein endothelial cells (HUVECs; CC-2517) were purchased from Lonza Group Ltd (Basel, Switzerland). POAECs and HOAECs were cultured and maintained in tissue culture medium from (Cell Application Inc. San Diego, Calif. USA); whereas HUVECs were cultured and maintained in tissue culture medium purchased from (GIBCO, USA). Cells were used from passage 2-10 in all experiments at a split ratio of 1:3. To test that endothelial cells were not activated during culture, IL1-levels in conditioned medium were measured using ELISA (R&D Systems, MN.), and were consistently found to be negligible (<4 pg/ml).
Human peripheral blood neutrophils were prepared by dextran sedimentation of heparinized whole blood obtained from healthy donors and centrifuged through Ficoll-Paque as described previously [16]. Contaminating red blood cells were removed by hypotonic lysis with isotonic NH4Cl. The remaining cells were suspended in Krebs-HEPES medium (pH 7.4) containing 120 mM NaCl, 1.3 mM CaCl2, 1.2 mM MgSO4, 4.8 mM KCl, 1.2 mM KH2PO4, 25 mM HEPES and 0.1% Bovine serum albumin (BSA) and were further purified through neutrophil isolation medium (Cardinal Associates, Santa Fe, N. Mex.). Final purity and viability were both between 98-99% as indicated by flow cytometry and trypan blue dye exclusion tests. Neutrophils were routinely tested for production of reactive oxygen metabolites (ROM) by luminol-dependent chemiluminescence (LDCL) for 10 minutes. Cells were considered naive and therefore suitable for experimentation only when no increase in LDCL was observed.
Acute promyelocytic lukemia; HL-60 cell line (Catalog No.CCL-240), acute mylogenous Lukemia; KG-1 cell line (Catalog No.CCL-246) and acute monocytic leukemia; THP-1 cell line (Catalog No.TIB-202) were purchased from ATCC (ATCC, Rockville, Md.). HL-60 and KG-1 cell lines were cultured in complete Iscoves Modified Medium (ATCC catalog No. 30-2005) supplemented with 10% fetal bovine serum (ATCC catalog No. 30-2020) and penicillin (100 U/ml), and streptomycin (100 μg/ml). THP-1 cells were cultured in complete RPMI media (ATCC catalog No. 30-2001) supplemented with 10% Fetal bovine serum (ATCC catalog No. 30-2020) and penicillin (100 U/ml), and streptomycin (100 μg/ml). All cell lines were maintained in a humidified incubator at 37° C. with 5% CO2. HL-60 differentiation into neutrophil-like cells was performed by treatment of 2×106 cell/ml with 1.3% DMSO (Sigma catalog No. D4540) in complete media for 6-8 days with media change every third day. Differentiation into neutrophil-like cells was ascertained by their ability to generate Reactive Oxygen Metabolite (ROM) in response to stimulation by phorbol myristate acetate; PMA (100 ng/ml) or the chemotactic peptide fMLP (1 μM). This was detected by either the reduction of the soluble NBT to blue-black insoluble formazan and/or Lumiol-dependent chemilumesicence. For the former, one ml of cell suspension was incubated for 20 min at 37° C. with an equal volume of 0.2% NBT (Sigma Chemical Co., St. Louis, Mo.) dissolved in phosphate-buffered saline (pH 7.2; 0.15 M without Ca+2, Mg+2), in the presence of 200 ng of PMA. Differentiated cells contain formazan deposits as dark, irregularly shaped crystal inclusions in the cytoplasm. By Day 6, approximately 98% of the cells reduced NBT upon PMA stimulation, and less than 5% in the absence stimulation. THP-1 and KG-1 differentiation was performed as above but with treatment with Bt2cAMP (500 n/ml) and PMA (100 ng/ml) for four (4) days and five (5) days, respectively [18]. Differentiation was confirmed by ROM production as above.
Anti-Gal(1,3) gal antibodies were prepared essentially as described previously [19] and all proceedures approved by the Animal Care and Use Committee (IRB at KFSHRC). Briefly, 10-15-kg non human promates were immunized by intra-muscular injection of emulsified soluble Gal(1,3) gal with Hunter's TiterMax Adjuvant (Sigma, USA). The animals were given booster injections 3 weeks later. Samples of blood were taken at 5 weeks postimmunization and tested for binding to porcine thyroglobulin, soluble Gal(1,3) gal and PAECs as described previously [30]. Booster injections were given at 4-6 weeks thereafter and continued for 6-9 months. To obtain Gal(1,3) gal antiserum blood was collected in 50-ml sterile Falcon tubes and allowed to clot at room temperature for 30 min. Serum was centrifuged (3000 g, 4° C., 30 min) heat-inactivated (30 min, 56° C.), and recentrifuged (1000 g, 4° C., 30 min). Antiserum immunoglobulins (IgG, IgA and IgM) were quantified using Cobas Mira Plus System (Hoffmann-La Roche, Basel, Switzerland) before extensive dialysis against 5 mM sodium phosphate buffer (pH 6.5). The dialysate was applied to equilibrated anion resin (Sephadex DEAE A-50, Pharmacia, Uppsala, Sweden) at a ratio of 2:1 (resin:supernatant). The use of this anion resin ensured that essentially all serum protein component except IgG bind to the resin, leaving an eluate rich in IgG. The eluate was fractionated by ion-exchange chromatography on Sephadex DEAE A-50. Purified fractions were pooled, dialyzed against PBS and concentrated.
F(ab)2 fragments of anti-Gal(1,3) gal IgG were prepared by papain digestion. Fifty microlitre (50 μl) of papain solution (10 mg/ml in 0.1 M sodium phosphate buffer, pH 7.0) were added to 50 mg/ml of IgG in 3 ml of PBS. The digestion mixture was incubated at 37° C. for 4 hrs. The hydrolysed product was dialyzed first against Mill-Q water then against 0.01M sodium acetate buffer (pH 5.5). Samples were removed and fractionated on a Sephacryl-S-200 column (Pharmacia). Blocking experiments with Gal(1,3) gal IgG were performed as follows: PAECs were trypsinized by incubation with Trypsin-EDTA solution for endothelial cell culture (Sigma. USA) for 2 min. at 37° C. The cells were washed three times with RPMI 1640 medium (Sigma. USA). The washed cells were then incubated with 100 g/ml of the Gal(1,3) gal IgG or F(ab)2 fragments of the antibodies at room temperature for 30 min. The suspension was then added to adherent neutrophils at a final ratio of 10:1 (neutrophils to PAECs). This concentration was previously shown to sufficiently block all Gal(1,3) gal binding sites [16].
Neutrophils or appropriate differentiated cell lines were loaded with Fluo-3-AM (1 μM) as described previously [17]. The cells were washed, placed on glass coverslips and allowed to adhere for 15 minutes at room temperature. Coverslips were washed then secured between two plates of a custom-designed coverslip holder, placed onto a heated microscope stage (37° C.) and [Ca++]i images were acquired at 1-2 seconds intervals. For each coverslip 100 μl of POAECs, suspended in Krebs-Hepes buffer (pH 7.4), containing 104 cells were added and image acquisition was continued for at least 5 minutes. Control experiments were carried out using equal number of HOAECs or HUVECs/coverslip. Images were analyzed using UltraView confocal software (PerkinElmer, UK) and fluorescence intensity (from each cell) was transformed into absolute calcium levels as described previously [16]. Because undifferentiated cell lines were none adherent, calcium measurements were carried out using fluorimetric assays (PerkinElmer LS 55 Luminescence Spectrometer, PerkinElmer, UK) with cells labeled with fura-2 AM as described previously [20]. Experiments were analyzed using FL WinLab software (PerkinElmer, UK).
The production of Reactive Oxygen Metabolites (ROM) by neutrophils and the three cell lines were measured using luminol-dependent chemiluminescence (LDCL) on an FB12 single tube luminometer (Berthold Detection Systems, Titertek Instrument, Inc., Huntsville, USA), as essentially described previously [15]. Briefly 1.5 ml of cells (suspended in Krebs-Hepes, pH 7.4) containing 106 cells were challenged with 150 μl containing 104 PAECs (suspended in Krebs-Hepes buffer, pH 7.4) and LDCL was followed for 15 minutes. For control experiments PAECs were replaced with HOAECs or HUVECs.
Total cellular RNA was isolated from (1-2)×107 differentiated/undifferentiated cell lines and human naïve neutrophils using tri-Reagent (MRC, Cincinati, Ohio) following manufacturer's instructions. RNA integrity was routinely checked using 500 ng/ml of RNA on 1% denaturing agarose gel.
SAGE was performed according to the Serial Analysis of Gene Expression detailed Protocol Version C, and analyzed using SAGE analysis software version 4.5 (Johns Hopkins University, Baltimore, Md., USA). In brief, Ten micrograms (10 μg) of total RNA was bound to solid phase oligo (dT) magnetic beads. The cDNA was synthesized directly on the oligo(dT) bead. Oligo(dT) bound to magnetic beads was used as a template for the first strand cDNA synthesis, followed by the second-strand cDNA synthesis. The captured cDNAs were then digested with an “anchoring” restriction enzyme, Nla III, which left a 3′ overhang. Complementary cDNA synthesis and Nla III digestion was verified using PCR. The 3′ fragments were then isolated using the magnetic beads, and equally divided into two pools and ligated to two different linkers, A or B. Both linkers contain the recognition sequence for a “tagging” restriction enzyme (type IIs restriction enzyme) Mme. The tagging enzyme produced a staggered cut, offset by about 17 bp 3′ from the recognition sequence. The two linkers were ligated onto the Nla III overhangs. The efficiency of ligation was assessed by PCR. Subsequent digestion with Mme released the adapter with a short tag of cDNA from the beads. These tags were then ligated tail-to-tail, to form 130-bp ditags. The resulting ditags were PCR amplified using primers specific to each linkers, pooled, precipitated and gel purified. The linkers were released by digesting with NlaIII, and the resulting 34-bp ditags were gel purified, concatenated and resolved on 8% (w/v) polyacrylamide gel. The high molecular weight bands (300-500 bp, 500-800 bp, and 800 bp-1 kb) were gel purified, and cloned into Sph1-linearized pZero-1 vector (Invitrogen, Carlsbad, Calif., USA). Ligation products were transformed into One Shot TOP10 electrocompetent cells. Transforments were analyzed by colony PCR. Approximately 4000-5000 clones for each library were cycle sequenced using M13 forward primer and analyzed on Applied Biosystems DNA Sequencer. Each concatamer insert results in a randomly organized “series” of ditags of approx 34 bp, each flanked by the recognition sequence of the primary anchoring enzyme NlaIII, CATG sequence that provide a “SAGE tag” specific to each expressed gene. Approximately 20-25 individual tags were were produced per clone. SAGE software was used to convert these sequences into long SAGE tags and tabulated tag abundances. Resultant SAGE tags were analyzed using the downloadable reference sequence database SAGEmap (Lash A. E et al, 2000) from the NCBI Web site. By determining the frequency distribution of the total tag population, the statistical picture of the relative abundance of the different mRNAs expressed in the differentiated vs undifferentiated cell population was obtained. Using this method (SAGE raw 17mer data) we generated five libraries, for human naïve neutrophils, differentiated and undifferentiated HL60 and KG1 Cell lines. Whereas the 10-mer tag count and differential expression results for THP-1 cells were from the GEO data repository at NCBI (accession # GSE1439). All 17- and 10 mer SAGE tags identified for the three cell lines and raw tag counts were aggregated for each gene across multiple tags. Differential expression significance for these aggregated counts was determined using a z-test, where z=(xd−xu)/v(xd+xu), and p-values assigned as <0.01 for z>2.58 and <0.05 for z>1.96, according to a univariate normal distribution. Subsequently differentially expressed genes in all three cell lines (p-value<0.05) were considered.
1.10 Quantification of Specific Transcripts with LightCycler RT-PCR.
Total RNA was prepared by the guanidine isothiocyanate method using TRI REAGENT (Sigma, USA) according to the manufacturer's instructions. The RNA concentration was measured by microspectrophotometry (NanoDrop Technologies, Wilmington, Del.). cDNA was synthesized from the total RNA using AMV Reverse Transcriptase (Promega, Wis., USA) according to the manufacturers protocol. cDNA synthesis were performed in a final volume of 20 μl. Briefly, 2 μl of (1:10dil) of the cDNA were used for amplification in the SYBRgreen format using the LightCycler FastStart DNA Master SYBRGreen I kit (Roche Diagnostics, catalog no. 2 239 264). Primers derived from the human gene sequence were designed using the Oligo 6 Primer analysis software (Applied Biosystems, Foster City, Calif.). Mastermixes for human CD82 and GAPDH mRNA, and porcine alpha-GAL transferase and GAPDH mRNA were prepared according to the manufacturer's instructions, using the following primer sets:
Quantitative PCR was performed using the LightCycler 480 system (Roche Diagnostics, Mannheim, Germany). Briefly, to the 8 μl of LightCycler mastermix a maximum of 10 ng cDNA in a 2 μl volume was added as PCR template. A no-target control received 8 μl of reaction mixture with 2 μl of water. Sealed capillaries were centrifuged (5 s at 1000 rpm) using the LightCycler centrifuge adapters and placed into the LightCycler rotor. PCR amplification was performed in triplicate wells. The following temperature profile was utilized for amplification: denaturation for 1 cycle at 95° C. for 30 s and 40 cycles at 95° C. for 10 s (temperature transition, 20° C./s), 64 to 50° C. (step size, 1° C.; step delay, 5 cycle) for 15 s (temperature transition, 20° C./s), and 72° C. for 15 s (temperature transition, 2° C./s) with fluorescence acquisition at 55 to 50° C. in single mode. Melting-curve analysis was done at 45° C. to 90° C. (temperature transition, 0.2° C./s) with continuous fluorescence acquisition. Sequence-specific standard curves were generated using 10-fold serial dilutions (102 to 108 copies/μl) of known amounts of cDNA. The respective concentration for any given sample was calculated using crossing cycle analysis provided by the LightCycler software. For realistic quantifications, the start amount of RNA was the same for all samples. Minor sampling errors were avoided by normalization with the housekeeping gene G3PDH.
Immunofluorescence was performed essentially as described previously [16]. Briefly, 50 μl of live cell suspension (107 cells/ml) were incubated primary antibodies at 1:250 dilution for one hour on ice. Cells were washed and treated with secondary antibodies at 1:500 dilution for 1 hour on ice. Cells were washed and spotted on the center of a coverslip which was sandwiched between two plates of specially designed holder and viewed using Zeiss Meta 510 Confocal Microscope (Zeiss, Jena, Germany). The same antibodies were used for POAECs CD82 immunofluorescence.
When human naive neutrophils were exposed to POAECs (2×106/ml), their intracellular free calcium concentrations [Ca++]i rose from the resting level of 70±0.1 nM to 499±33 nM before decaying back to pre POAECs encounter (
2.2 Activation of Human NaïVe Neutrophils by Xenogeneic Endothelial Cells but not Allogeneic Endothelial Cells:
Activation of human naïve neutrophils following xenogeneic encounter was tested by measuring reactive oxygen metabolite (ROM) production using Luminol-Dependent Chemilumenescence (LDCL). In a series of experiments we found that POAECs cells invoked ROM production in human naïve neutrophils (
2.3 Undifferentiated Human Cell Lines HL-60, THP-1 and KG-1 do not Recognize Xenogeneic Endothelium Unless Differentiated into Neutrophil-Like or Monocyte-Like Cells:
Since both wild-type and α-gal-knockout xenogeneic endothelial cells were recognized by human naïve neutrophils and since the latter are terminally differentiated thus possess all the necessary components for such recognition, we investigated the ability of less differentiated human derived cell lines to recognize xenogeneic endothelial cells. We tested three myeloid leukemic cell lines; HL60 and THP-1 which differentiate into neutrophil-like cells, and KG-1 which differentiate into monocyte-like cells, respectively [2]-24]. The undifferentiated promyeloblast cell line HL-60 assumes a nonadherent spherical morphology which changes into a neutrophil-like phenotype, with adhesive capabilities upon differentiation in 1.25% DMSO for 7 days. Using a ratiometric calcium dye Fura-2-AM labeled undifferentiated the HL-60 cell suspension, we found that POAECs were unable to evoke a significant calcium rise in HL60 cell suspension (
Since only differentiated cell lines and terminally differentiated neutrophils were able to recognize the xenogeneic POAECs, the possibility existed that common molecular moiety(s) in the four cell types may be responsible for this recognition. We therefore used Serial Analysis of Gene Expression (SAGE) to identify the differentially expressed transcript(s) in the three cell lines and in human naive neutrophils. We used a snap shot approach of using mRNA transcripts of undifferentiated and post differentiation of HL-60 and KG-1 cells, within which our recognition moiety(s) were expected to exist. Undifferentiated HL-60 exhibited 14578 transcripts after sequencing 20261 tags, whereas differentiated HL60 exhibited 16277 transcripts following 18206 sequenced tags (
2.5 Confirmation of SAGE Results at the mRNA and Protein Levels:
To confirm the differential expression of CD82 transcripts we used qRT-PCR and western blot analysis on samples from undifferentiated and differentiated cell lines and human naive neutrophils. We found that in the undifferentiated cells, the ratio of CD82 mRNA transcript relative to the GAPDH was 2.40±0.03, and this ratio rose to 20.74±0.13 upon differentiation. Similar results were obtained in the other two cell lines, namely, KG-1 and THP-1 (
Since SAGE, qRT-PCR, western and confocal data have identified CD82 as the likely candidate for xenogeneic recognition, we argued that blocking CD82 by anti CD82 antibodies should inhibit recognition of POAECs by human naive neutrophils. In a series of experiments we have exposed the latter cell type to anti-CD 82 antibodies (1 μg/ml for 15 minutes at RT) prior to xenogeneic contact. We found that treatment with anti CD82 antibodies significantly (p<0.0001) reduced POAECs-induced calcium rise in human naïve neutrophils from 482±24 nM to 183±12 nM (
The features disclosed in the foregoing description, in the claims and/or in the accompanying drawings may, both separately and in any combination thereof, be material for realizing the invention in diverse forms thereof
