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Paper · 305458

Genetic restrictions for the induction of suppressor T cells by hapten-modified lymphoid cells in tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity. Role of the H-2D region of the major histocompatibility complex.

Miller SD and 2 others. J Exp Med, 1978. Cited by 67 papers, by iCite.

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ConductScience Library. Genetic restrictions for the induction of suppressor T cells by hapten-modified lymphoid cells in tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity. Role of the H-2D region of the major histocompatibility complex. Papers, record 305458. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/305458

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Paper

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

Title
Genetic restrictions for the induction of suppressor T cells by hapten-modified lymphoid cells in tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity. Role of the H-2D region of the major histocompatibility complex.
PubMed
Journal
J Exp Med
PubMed
Year
1978
PubMed
Publication types
Journal Article, Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
67
iCite
Relative citation ratio, by iCite
1.43
iCite
Revised in PubMed
2021-12-03
PubMed

Authors3

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

OrderAuthorForenameKindORCID iD
1Miller SDS D
2Sy MSM S
3Claman HNH N

Source PubMed

Topics13

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

MeSH termMajor
DinitrofluorobenzeneMajor topic
H-2 AntigensMajor topic
Immunity, CellularMajor topic
Immunosuppression TherapyMajor topic
NitrobenzenesMajor topic
T-LymphocytesMajor topic
Animals
Chromosome Mapping
Dermatitis, Contact
Dinitrobenzenes
Haptens
Immune Tolerance
Mice

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.

References25

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

OrderPMIDTitleJournalYearIn PapersSource
1302,178Genetic restriction in T-lymphocyte activation by antigen-pulse peritoneal exudate cells.Cold Spring Harb Symp Quant Biol1977https://conductscience.org/library/papers/302178PubMed
2300,292Tolerance and contact sensitivity to DNFB in mice. VII. Functional demonstration of cell-associated tolerogen in lymph node cell populations containing specific suppressor cells.Cell Immunol1977https://conductscience.org/library/papers/300292PubMed
3300,774H-2 restriction of suppressor T-cell induction by hapten-modified lymphoid cells in tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitization.J Exp Med1977https://conductscience.org/library/papers/300774PubMed
4301,091The induction of hapten-specific T cell tolerance using hapten-modified lymphoid membranes. II. Relative roles of suppressor T cells and clone inhibition in the tolerant state.Eur J Immunol1977https://conductscience.org/library/papers/301091PubMed
5299,922H-2 compatibility requirements for T suppressor cell functions induced by Friend leukaemia virus.Nature1977https://conductscience.org/library/papers/299922PubMed
6915,281Soluble factors in tolerance and contact sensitivity to DNFB in mice. II. Genetic requirements for suppression of contact sensitivity by soluble suppressor factor.J Immunol1977https://conductscience.org/library/papers/915281PubMed
7874,422Suppressor cells in tolerance to contact sensitivity active against hapten-syngeneic and hapten-allogeneic determinants.J Exp Med1977https://conductscience.org/library/papers/874422PubMed
8874,323
Soluble factors in tolerance and contact sensitivity to 2,4-dinitrofluorobenzene in mice. I. Suppression of contact sensitivity by soluble suppressor factor released in vitro by lymph node cell populations containing specific suppressor cells.
J Immunol1977https://conductscience.org/library/papers/874323PubMed
91,087,316The induction of hapten-specific T cell tolerance by using hapten-modified lymphoid cells. I. Characteristics of tolerance induction.J Immunol1976https://conductscience.org/library/papers/1087316PubMed
101,085,418Separation of suppressor and killer T cells by surgace phenotype.Nature1976https://conductscience.org/library/papers/1085418PubMed

Cited by13

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 67 citations.

PMIDTitleJournalYearIn PapersSource
8,001,023Effect of murine interferon alpha/beta on tumour-induced suppressor function.Cancer Immunol Immunother1994https://conductscience.org/library/papers/8001023PubMed
7,203,554Analysis of neonatally induced tolerance of H-2 alloantigens. I. Adoptive transfer indicates that tolerance of class I and class II antigens is maintained by distinct mechanisms.Immunogenetics1981https://conductscience.org/library/papers/7203554PubMed
6,449,479Suppression of the proliferative response to H-2D by I-J subregion gene products.Immunogenetics1980https://conductscience.org/library/papers/6449479PubMed
6,444,234Role of self carriers in the immune response and tolerance. V. Reversal of trinitrophenyl-modified self suppression of the B-cell response by blocking of H-2 antigens.J Exp Med1980https://conductscience.org/library/papers/6444234PubMed
6,242,890Serological detection of H-2K- and H-2D-gene products. I. Principal difference between T and B lymphocytes in expression of H-2D-encoded alloantigens.Immunogenetics1980https://conductscience.org/library/papers/6242890PubMed
6,214,508Genetic regulation of the antibody response to H-2Db alloantigens in mice. V. Control by several genes of the H-2 complex in mice of the C57BL/10 background.Immunogenetics1982https://conductscience.org/library/papers/6214508PubMed
6,193,239An antigen-specific signal is required for the activation of second-order suppressor T cells in the regulation of delayed-type hypersensitivity to 2,4,6-trinitrobenzene sulfonic acid.J Exp Med1983https://conductscience.org/library/papers/6193239PubMed
6,165,799Antigen- and receptor-driven regulatory mechanisms. VII. H-2-restricted anti-idiotypic suppressor factor from efferent suppressor T cells.J Exp Med1981https://conductscience.org/library/papers/6165799PubMed
3,785,166Regulated expression of a murine class I gene in transgenic mice.Mol Cell Biol1986https://conductscience.org/library/papers/3785166PubMed
3,159,824
Tubular antigen-derivatized cells induce a disease-protective, antigen-specific, and idiotype-specific suppressor T cell network restricted by I-J and Igh-V in mice with experimental interstitial nephritis.
J Exp Med1985https://conductscience.org/library/papers/3159824PubMed

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Genes0

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

None in this release.

Drugs0

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None in this release.

Data0

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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

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  • ClinicalTrials.govNo license stated
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  • 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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