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Paper · 306407

Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. I. Failure to collaborate with B cells of the opposite parental strain not associated with active suppression.

Sprent J. J Exp Med, 1978. Cited by 89 papers, by iCite.

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ConductScience Library. Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. I. Failure to collaborate with B cells of the opposite parental strain not associated with active suppression. Papers, record 306407. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/306407

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Paper

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

Title
Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. I. Failure to collaborate with B cells of the opposite parental strain not associated with active suppression.
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
89
iCite
Relative citation ratio, by iCite
1.66
iCite
Revised in PubMed
2021-12-03
PubMed

Authors1

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

OrderAuthorForenameKindORCID iD
1Sprent JJ

Source PubMed

Topics14

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

MeSH termMajor
Antibody FormationMajor topic
B-LymphocytesMajor topic
Lymphocyte ActivationMajor topic
Lymphocyte CooperationMajor topic
T-LymphocytesMajor topic
Animals
Dose-Response Relationship, Immunologic
Erythrocytes
Hemagglutinins
Heterozygote
Immunosuppression Therapy
Macrophages
Mice
Spleen

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.

References20

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

OrderPMIDTitleJournalYearIn PapersSource
1233,906Independent populations of primed F1 guinea pig T lymphocytes respond to antigen-pulsed parental peritoneal exudate cells.J Exp Med1977https://conductscience.org/library/papers/233906PubMed
262,818Nature of the antigenic complex recognized by T lymphocytes. I. Analysis with an in vitro primary response to soluble protein antigens.J Exp Med1976https://conductscience.org/library/papers/62818PubMed
367,169T-T interactions in the induction of suppressor and helper T cells: analysis of membrane phenotype of precursor and amplifier cells.J Exp Med1977https://conductscience.org/library/papers/67169PubMed
420,229Induction of H-2-restricted cytotoxic T cells: in vivo induction has the appearance of being unrestricted.Cell Immunol1977https://conductscience.org/library/papers/20229PubMed
514,486Ionizing radiation and the immune response.Adv Immunol1976https://conductscience.org/library/papers/14486PubMed
6301,903Haplotype preference in lymphocyte differentiation. I. Development of haplotype-specific helper and suppressor activities in F1 hybrid-activated T cell populations.J Immunol1977https://conductscience.org/library/papers/301903PubMed
74,400,172Specific unresponsiveness of recirculating lymphocytes ater exposure to histocompatibility antigen in F 1 hybrid rats.Nat New Biol1971https://conductscience.org/library/papers/4400172PubMed
84,108,546Activation of thymus cells by histocompatibility antigens.Nat New Biol1971https://conductscience.org/library/papers/4108546PubMed
94,399,170Antigen-induced selective recruitment of circulating lymphocytes.Cell Immunol1971https://conductscience.org/library/papers/4399170PubMed
1052,686Collaboration of allogeneic T and B lymphocytes in the primary antibody response to sheep erythrocytes in vitro.J Exp Med1975https://conductscience.org/library/papers/52686PubMed

1 to 10 of 20

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Cited by32

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 89 citations.

PMIDTitleJournalYearIn PapersSource
29,148,973The somatically generated portion of T cell receptor CDR3α contributes to the MHC allele specificity of the T cell receptor.Elife2017https://conductscience.org/library/papers/29148973PubMed
22,345,700Positive selection in the thymus: an enigma wrapped in a mystery.J Immunol2012https://conductscience.org/library/papers/22345700PubMed
9,177,213The peripheral blood fibrocyte is a potent antigen-presenting cell capable of priming naive T cells in situ.Proc Natl Acad Sci U S A1997https://conductscience.org/library/papers/9177213PubMed
7,276,826
Antigen recognition. V. Requirement for histocompatibility between antigen-presenting cell and B cell in the response to a thymus-dependent antigen, and lack of allogeneic restriction between T and B cells.
J Exp Med1981https://conductscience.org/library/papers/7276826PubMed
7,026,722
Role of the major histocompatibility complex in T cell activation of B cell subpopulations. Major histocompatibility complex-restricted and -unrestricted B cell responses are mediated by distinct B cell subpopulations.
J Exp Med1981https://conductscience.org/library/papers/7026722PubMed
7,021,751
Role of the major histocompatibility complex in T cell activation of B cell subpopulations Lyb-5+ and Lyb-5- B cell subpopulations differ in their requirement for major histocompatibility complex-restricted T cell recognition.
J Exp Med1981https://conductscience.org/library/papers/7021751PubMed
6,966,313
Induction of tolerance to 1-fluoro-2,4-dinitrobenzene contact sensitivity with hapten-modified lymphoid cells. II. Selective tolerance in F1 mice of T cell subsets recognizing 1-fluoro-2,4-dinitrobenzene associated with parental major histocompatibility complex antigens.
J Exp Med1980https://conductscience.org/library/papers/6966313PubMed
6,813,419Genetic control of immune response to myoglobin. Ir gene function in genetic restriction between T and B lymphocytes.J Exp Med1982https://conductscience.org/library/papers/6813419PubMed
6,602,200Role of interleukin 1 in anti-immunoglobulin-induced B cell proliferation.J Exp Med1983https://conductscience.org/library/papers/6602200PubMed
6,455,762T cell recognition of antigen in vivo: role of the H-2 complex.Springer Semin Immunopathol1980https://conductscience.org/library/papers/6455762PubMed

1 to 10 of 32

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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

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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