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Paper · 6200565

Antigen-specific suppression of human antibody responses by allogeneic T cells. I. Frequency and antigen specificity of allogeneic suppressor T cells and their role in major histocompatibility complex-controlled genetic restriction.

Callard RE and 2 others. J Exp Med, 1984. Cited by 10 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Antigen-specific suppression of human antibody responses by allogeneic T cells. I. Frequency and antigen specificity of allogeneic suppressor T cells and their role in major histocompatibility complex-controlled genetic restriction. Papers, record 6200565. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/6200565

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Paper

PubMed's record of the paper, with iCite's citation figures. No abstract is shown.

Title
Antigen-specific suppression of human antibody responses by allogeneic T cells. I. Frequency and antigen specificity of allogeneic suppressor T cells and their role in major histocompatibility complex-controlled genetic restriction.
PubMed
Journal
J Exp Med
PubMed
Year
1984
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
10
iCite
Relative citation ratio, by iCite
0.28
iCite
Revised in PubMed
2019-05-08
PubMed

Authors3

The authors in the order PubMed's record lists them, with the ORCID iDs it states.

OrderAuthorForenameKindORCID iD
1Callard RER E
2Winger CMC M
3Tiernan SLS L

Source PubMed

Topics13

NLM's MeSH indexing of the paper, its major topics first.

MeSH termMajor
EpitopesMajor topic
Genes, MHC Class IIMajor topic
Lymphocyte CooperationMajor topic
T-Lymphocytes, RegulatoryMajor topic
Antibody-Producing Cells
HLA Antigens
Hemolytic Plaque Technique
Humans
Immunoglobulins
Lymphocyte Activation
Phenotype
T-Lymphocytes, Cytotoxic
T-Lymphocytes, Helper-Inducer

Source PubMed

Grants0

Each grant PubMed's record writes, matched to the NIH project NIH's grant and paper links name for this paper, and each of those links the record does not write.

None in this release.

Trials0

The trials whose ClinicalTrials.gov record lists the paper, and the trial numbers the paper's PubMed record names.

None in this release.

Comments and corrections0

PubMed's comments and corrections, NLM's own indexing: retractions first, then expressions of concern, errata and updates, and comments last.

None in this release.

References33

The papers the reference list in PubMed's record names, those in our copy of PubMed, in the list's order.

OrderPMIDTitleJournalYearIn PapersSource
15,001,843Antigen binding cells in tolerance and immunity.Transplant Rev1970https://conductscience.org/library/papers/5001843PubMed
24,943,147Infectious immunological tolerance.Immunology1971https://conductscience.org/library/papers/4943147PubMed
34,641,854Inhibitory and stimulatory effects of concanavalin A on the response of mouse spleen cell suspensions to antigen. I. Characterization of the inhibitory cell activity.J Exp Med1972https://conductscience.org/library/papers/4641854PubMed
44,583,095Depression of the T cell phenomenon of contact sensitivity by T cells from unresponsive mice.Nature1973https://conductscience.org/library/papers/4583095PubMed
54,600,315An improved rosetting assay for detection of human T lymphocytes.J Immunol Methods1974https://conductscience.org/library/papers/4600315PubMed
64,276,949Cell-mediated immune responses in vitro. I. Suppression of the generation of cytotoxic lymphocytes by concanavalin A and concanavalin A-activated spleen cells.J Exp Med1974https://conductscience.org/library/papers/4276949PubMed
74,279,271Regulatory mechanisms in cell-mediated immune responses. I. Regulation of mixed lymphocyte reactions by alloantigen-activated thymus-derived lymphocytes.J Exp Med1974https://conductscience.org/library/papers/4279271PubMed
814,213Suppressor T cells arising in mice undergoing a graft-vs-host response.J Immunol1977https://conductscience.org/library/papers/14213PubMed
9325,144Negative allogeneic effects in vitro. I. Allogeneic T cells markedly suppress the secondary antibody-forming cell response.J Immunol1977https://conductscience.org/library/papers/325144PubMed
10301,501Co-operation across histocompatibility differences. The role of inhibitory T cells in preventing successful T-B interaction.Immunology1977https://conductscience.org/library/papers/301501PubMed

Cited by4

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 10 citations.

PMIDTitleJournalYearIn PapersSource
6,236,916Relative sensitivity of human T cell subsets to deoxyadenosine toxicity.Clin Exp Immunol1984https://conductscience.org/library/papers/6236916PubMed
3,493,099The effect of iron (Fe3+) on the cloning efficiency of human memory T4+ lymphocytes.Clin Exp Immunol1986https://conductscience.org/library/papers/3493099PubMed
2,959,615Specific antibody responses by high- and low-density human peripheral blood B cells: T-helper cells and T-cell replacing factor (TRF) act on different B-cell subpopulations.Immunology1987https://conductscience.org/library/papers/2959615PubMed
2,784,736Limit dilution analysis of peripheral blood T lymphocytes specific to periodontopathic bacteria.Clin Exp Immunol1989https://conductscience.org/library/papers/2784736PubMed

Genes1

The genes the Gene search release ties to the paper: Swiss-Prot's references first, then PubTator's text mining.

GeneNCBI Gene IDLinked byIn Genes
HLA-A3,105PubTator's text mininghttps://conductscience.org/library/genes/3105

Source NCBI Gene

Drugs0

The drugs whose trials, in the Pipelines release, list the paper.

None in this release.

Data0

The data bank entries PubMed's record names. Trial numbers are under Trials.

None in this release.

Data dates

The date of each source this release read.

PubMed
2026-11-06
PubMed
iCite
2026-11-05
iCite
PMC's ID file
2026-11-05
PMC's ID file
NIH RePORTER's grant and paper links
2026-11-01
NIH RePORTER's grant and paper links
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
Each source's terms
  • 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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