Paper · 53263
The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens.
Bevan MJ. J Exp Med, 1975. Cited by 551 papers, by iCite.
11 sourcespapers-2026-11-12-0.1.0
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ConductScience Library. The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens. Papers, record 53263. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/53263
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Paper
PubMed's record of the paper, with iCite's citation figures. No abstract is shown.
- Title
- The major histocompatibility complex determines susceptibility to cytotoxic T cells directed against minor histocompatibility antigens.
- PubMed
Topics15
NLM's MeSH indexing of the paper, its major topics first.
| MeSH term | Major |
|---|---|
| Genes | Major topic |
| Histocompatibility | Major topic |
| T-Lymphocytes | Major topic |
| Animals | |
| Cell Line | |
| Cytotoxicity Tests, Immunologic | |
| Epitopes | |
| Histocompatibility Antigens | |
| Isoantigens | |
| Mice | |
| Mice, Inbred BALB C | |
| Mice, Inbred Strains | |
| Species Specificity | |
| Spleen | |
| Transplantation, Homologous |
Source PubMed
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Trials0
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Comments and corrections0
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References24
The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.
| Order | PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|---|
| 1 | 49,564 | A biological role for the major histocompatibility antigens. | Lancet | 1975 | https://conductscience.org/library/papers/49564 | PubMed |
| 2 | 5,025,438 | Rejection of ascites tumor allografts. I. Isolation, characterization, and in vitro reactivity of peritoneal lymphoid effector cells from BALB-c mice immune to EL4 leukosis. | J Exp Med | 1972 | https://conductscience.org/library/papers/5025438 | PubMed |
| 3 | 5,682,942 | Quantitative studies on the mixed lymphocyte interaction in rats. 3. Kinetics of the response. | J Exp Med | 1968 | https://conductscience.org/library/papers/5682942 | PubMed |
| 4 | 1,078,719 | Genes required for cytotoxicity against virus-infected target cells in K and D regions of H-2 complex. | Nature | 1975 | https://conductscience.org/library/papers/1078719 | PubMed |
| 5 | 1,079,924 | Interaction antigens detected by cytotoxic T cells with the major histocompatibility complex as modifier. | Nature | 1975 | https://conductscience.org/library/papers/1079924 | PubMed |
| 6 | 1,086,219 | Cell-medicated cytotoxicity against ectromelia virus-infected target cells. III. Role of the H-2 gene complex. | Eur J Immunol | 1975 | https://conductscience.org/library/papers/1086219 | PubMed |
| 7 | 1,086,229 | Target cell-dependent T cell-mediated lysis of vaccinia virus-infected cells. | Eur J Immunol | 1975 | https://conductscience.org/library/papers/1086229 | PubMed |
| 8 | 1,090,698 | Cell interactions between histoincompatible T and B lymphocytes. VII. Cooperative responses between lymphocytes are controlled by genes in the I region of the H-2 complex. | J Exp Med | 1975 | https://conductscience.org/library/papers/1090698 | PubMed |
| 9 | 123,002 | H-2 compatibility is required for T-cell-mediated lysis of target cells infected with lymphocytic choriomeningitis virus. | J Exp Med | 1975 | https://conductscience.org/library/papers/123002 | PubMed |
| 10 | 123,256 | Alloimmune cytotoxic T cells: Evidence that they recognize serologically defined antigens and bear clonally restricted receptors. | J Immunol | 1975 | https://conductscience.org/library/papers/123256 | PubMed |
1 to 10 of 24
See all 24 referencesCited by135
The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 551 citations.
| PMID | Title | Journal | Year | In Papers | Source |
|---|---|---|---|---|---|
| 42,393,377 | A guide to CAR T cell therapies: development, current status and future prospects. | Nat Rev Immunol | 2026 | https://conductscience.org/library/papers/42393377 | PubMed |
| 34,485,921 | Engineering enhanced CAR T-cells for improved cancer therapy. | Nat Cancer | 2021 | https://conductscience.org/library/papers/34485921 | PubMed |
| 30,687,803 | Peter Doherty, Nobel Laureate: Questions and Reflections Concerning MHC Restriction and other Fruits of a Life of Biomedical Erudition. | Pathog Immun | 2018 | https://conductscience.org/library/papers/30687803 | PubMed |
| 30,479,379 | Models of immune selection for multi-locus antigenic diversity of pathogens. | Nat Rev Immunol | 2019 | https://conductscience.org/library/papers/30479379 | PubMed |
| 25,818,864 | Codification of bidentate pMHC interaction with TCR and its co-receptor. | Trends Immunol | 2015 | https://conductscience.org/library/papers/25818864 | PubMed |
| 25,750,245 | Medawar's legacy to cellular immunology and clinical transplantation: a commentary on Billingham, Brent and Medawar (1956) 'Quantitative studies on tissue transplantation immunity. III. Actively acquired tolerance'. | Philos Trans R Soc Lond B Biol Sci | 2015 | https://conductscience.org/library/papers/25750245 | PubMed |
| 22,457,925 | A new cytotoxic lymphocyte-defined antigen coded by a gene closely linked to the H-3 locus. | Immunogenetics | 1980 | https://conductscience.org/library/papers/22457925 | PubMed |
| 21,302,087 | Detection of two allotype-(Ig-1)-linked minor histocompatibility loci by the use ofH-2-restricted cytotoxic lymphocytes in congenic mice. | Immunogenetics | 1978 | https://conductscience.org/library/papers/21302087 | PubMed |
| 18,154,613 | Special regulatory T-cell review: Regulation of immune responses--examining the role of T cells. | Immunology | 2008 | https://conductscience.org/library/papers/18154613 | PubMed |
| 9,379,075 | Conformational changes in MHC class I molecules. Antibody, T-cell receptor, and NK cell recognition in an HLA-B7 model system. | Immunol Res | 1997 | https://conductscience.org/library/papers/9379075 | PubMed |
1 to 10 of 135
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- Trials
- 2026-11-12
- Gene search
- 2026-11-11
- Pipelines
- 2026-09-18
Sources 11
- ChEMBL, through Open TargetsCC BY-SA 3.0
- ClinicalTrials.govNo license stated
- HGNCCC0
- iCiteCC BY 4.0
- NCBI GenePublic domain (US government)
- NIH RePORTER's grant and paper linksPublic domain
- Open TargetsCC0 1.0
- PMC's ID filePublic domain (US government)
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0
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- ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- ClinicalTrials.govnone stated
- HGNCCC0: https://www.genenames.org/about/license/
- iCiteCC BY 4.0
- NCBI GeneNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- NIH RePORTER's grant and paper linksPublic domain (NIH RePORTER)
- Open TargetsCC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
- PMC's ID fileNone named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/
- PubMedNLM's terms
- PubTator 3Public domain
- UniProtCC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
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