CD8A
T-cell surface glycoprotein CD8 alpha chain
Also known as: CD8, CD8A_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P01732
- Gene
- CD8A
- Ensembl
- ENSG00000153563
- Chromosome
- 2
- Canonical length
- 235 aa
- Protein class
- CD markers, Disease related genes, Human disease related genes, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Plasma membrane
- Secretome location
- Intracellular and membrane
- Quaternary structure
- Homodimer
OverviewNCBI Gene
The CD8 antigen is a cell surface glycoprotein found on most cytotoxic T lymphocytes that mediates efficient cell-cell interactions within the immune system. The CD8 antigen acts as a coreceptor with the T-cell receptor on the T lymphocyte to recognize antigens displayed by an antigen presenting cell in the context of class I MHC molecules. The coreceptor functions as either a homodimer composed of two alpha chains or as a heterodimer composed of one alpha and one beta chain. Both alpha and beta chains share significant homology to immunoglobulin variable light chains. This gene encodes the CD8 alpha chain. Multiple transcript variants encoding different isoforms have been found for this gene. The major protein isoforms of this gene differ by the presence or absence of a transmembrane domain and thus differ in being a membrane-anchored or secreted protein. [provided by RefSeq, May 2020]
Canonical amino-acid sequenceUniProt
235 residues, UniProt reviewed canonical sequence.
>P01732|CD8A
1 MALPVTALLL PLALLLHAAR PSQFRVSPLD RTWNLGETVE LKCQVLLSNP TSGCSWLFQP
61 RGAAASPTFL LYLSQNKPKA AEGLDTQRFS GKRLGDTFVL TLSDFRRENE GYYFCSALSN
121 SIMYFSHFVP VFLPAKPTTT PAPRPPTPAP TIASQPLSLR PEACRPAAGG AVHTRGLDFA
181 CDIYIWAPLA GTCGVLLLSL VITLYCNHRN RRRVCKCPRP VVKSGDKPSL SARYVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CD8A can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.48
- Highest tissue expression
- 216 nTPM
Expression across tissuesHPA
Tissue
- thymus: 216 nTPM
- spleen: 94 nTPM
- lymph node: 28 nTPM
- small intestine: 17 nTPM
- appendix: 16 nTPM
- bone marrow: 14 nTPM
Single-cell type
- t-cells: 249 nCPM
- nk-cells: 36 nCPM
- pdcs: 15 nCPM
- lymphatic endothelial cells: 14 nCPM
- brain inhibitory neurons: 9.9 nCPM
- other brain neurons: 8.5 nCPM
Immune cell
- memory CD8 T-cell: 509 nTPM
- naive CD8 T-cell: 462 nTPM
- MAIT T-cell: 228 nTPM
- total PBMC: 149 nTPM
- gdT-cell: 29 nTPM
- NK-cell: 27 nTPM
Brain region
- cerebral cortex: 3.6 nTPM
- medulla oblongata: 3.5 nTPM
- pons: 2.5 nTPM
- spinal cord: 2.4 nTPM
- white matter: 2.4 nTPM
- basal ganglia: 2.2 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CD8A.
Disease | AllUniProt
Conditions CD8A is implicated in, by any mechanism.
- Immunodeficiency 116 (IMD116) MIM:608957
Disease | GeneticClinVar
2 pathogenic / likely-pathogenic of 218 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Susceptibility to respiratory infections associated with CD8alpha chain mutation
Disease | AutoantibodyPubMed
Conditions in which antibodies against CD8A are reported. Each links to that disease's full target list.
ReferencesPubMed · IEDB
Publications for CD8A from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
25 publications
- Inhibition of S-antigen induced experimental autoimmune uveoretinitis by oral induction of tolerance with S-antigen.
1990 · J Immunol · RCR 7.7 · 270 citations - Role of CD8+ T cells in mercury-induced autoimmunity or immunosuppression in the rat.
1990 · Scand J Immunol · RCR 1.5 · 53 citations - CD4+ T cells, but not CD8+ T cells, are required for the development of experimental autoimmune gastritis.
1998 · Immunology · RCR 1 · 56 citations - Chronic treatment of C3H-lpr/lpr and C3H-gld/gld mice with anti-CD8 monoclonal antibody prevents the accumulation of double negative T cells but not autoantibody production.
1994 · J Immunol · RCR 1 · 58 citations - Immunoregulation of mercuric chloride-induced autoimmunity in Brown Norway rats: a role for CD8+ T cells revealed by in vivo depletion studies.
1991 · Eur J Immunol · RCR 0.9 · 40 citations
Show 20 more
- Dysfunction of suppressor T cells in thyroid glands from patients with Graves' disease.
1987 · J Clin Endocrinol Metab · RCR 0.9 · 28 citations - Elevated Cerebrospinal Fluid Anti-CD4 Autoantibody Levels in HIV Associate with Neuroinflammation.
2022 · Microbiol Spectr · RCR 0.9 · 8 citations - In CD8+ T cell-deficient lpr/lpr mice, CD4+B220+ and CD4+B220- T cells replace B220+ double-negative T cells as the predominant populations in enlarged lymph nodes.
1995 · J Immunol · RCR 0.8 · 48 citations - Mercury-induced autoreactive anti-class II T cell line protects from experimental autoimmune encephalomyelitis by the bias of CD8+ antiergotypic cells in Lewis rats.
1993 · J Exp Med · RCR 0.8 · 37 citations - Effects of administration of monoclonal antibodies (anti-CD4 or anti-CD8) on the development of autoimmune diseases in (NZW x BXSB)F1 mice.
1998 · Immunobiology · RCR 0.7 · 37 citations - Involvement of PIT-1-reactive cytotoxic T lymphocytes in anti-PIT-1 antibody syndrome.
2014 · J Clin Endocrinol Metab · RCR 0.7 · 24 citations - Induction of T cell responses against autologous ovarian tumors with whole tumor cell lysate-pulsed dendritic cells.
2001 · Immunol Invest · RCR 0.6 · 30 citations - A distinct role of CD4+ Th17- and Th17-stimulated CD8+ CTL in the pathogenesis of type 1 diabetes and experimental autoimmune encephalomyelitis.
2011 · J Clin Immunol · RCR 0.5 · 23 citations - Combination of apoptotic T cell induction and self-peptide administration for therapy of experimental autoimmune encephalomyelitis.
2019 · EBioMedicine · RCR 0.5 · 12 citations - Generation and characterization of IL-2-activated veto cells.
1992 · J Immunol · RCR 0.5 · 21 citations - Inhibition of the development of spontaneous autoimmune thyroiditis in the obese strain (OS) chickens by in vivo treatment with anti-CD4 or anti-CD8 antibodies.
1998 · J Autoimmun · RCR 0.3 · 10 citations - Anti-CD8 treatment reduces the severity of inflammatory arthritis, but not vasculitis, in mercuric chloride-induced autoimmunity.
1996 · Clin Exp Immunol · RCR 0.3 · 12 citations - 4-1BB signaling breaks the tolerance of maternal CD8+ T cells that are reactive with alloantigens.
2012 · PLoS One · RCR 0.3 · 8 citations - Induction of unresponsiveness to Heymann's nephritis: inhibited by monoclonal antibody to CD4 but not to CD8.
1991 · Cell Immunol · RCR 0.2 · 10 citations - Regulation of the effector stages of experimental autoimmune encephalomyelitis via neuroantigen-specific tolerance induction. III. A role for anergy/deletion.
1998 · Autoimmunity · RCR 0.2 · 10 citations - Local immunomodulation with CD4 and CD8 antibodies, but not cyclosporine A, improves osteogenesis induced by ADhBMP9 gene therapy.
2005 · Gene Ther · RCR 0.2 · 8 citations - Human monoclonal rheumatoid factors augment arthritis in mice by the activation of T cells.
1996 · Clin Exp Immunol · RCR 0.1 · 3 citations - Movement disorders in encephalitis induced by Rhodococcus aurantiacus infection relieved by the administration of L-dopa and anti-T-cell antibodies.
1999 · Immunology · RCR 0.1 · 3 citations - [The effect of in vivo blockade of interleukin-1 and interferon-gamma on the autoimmune syndrom in the experimental model of graft versus host disease].
1994 · Srp Arh Celok Lek - A Granzyme B-Cleavable T Cell-Targeted Bispecific Cell Vesicle Connector for Reversing New-Onset Type 1 Diabetes.
2025 · J Am Chem Soc · 1 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.5
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adaptive immune response
- antigen processing and presentation
- cell surface receptor protein tyrosine kinase signaling pathway
- cell surface receptor signaling pathway
- immune response
- T cell activation
- T cell mediated immunity
- T cell receptor signaling pathway
- cytotoxic T cell differentiation
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CD8A in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CD8A as an antibody target. Whether an autoantibody or antibody against CD8A could matter depends on whether native CD8A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CD8A is annotated at the cell surface, where native CD8A is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CD8A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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