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Paper · 306408

Restricted helper function of F1 hybrid T cells positively selected to heterologous erythrocytes in irradiated parental strain mice. II. Evidence for restrictions affecting helper cell induction and T-B collaboration, both mapping to the K-end of the H-2 complex.

Sprent J. J Exp Med, 1978. Cited by 203 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. II. Evidence for restrictions affecting helper cell induction and T-B collaboration, both mapping to the K-end of the H-2 complex. Papers, record 306408. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/306408

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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. II. Evidence for restrictions affecting helper cell induction and T-B collaboration, both mapping to the K-end of the H-2 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
203
iCite
Relative citation ratio, by iCite
3.56
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

Topics15

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

MeSH termMajor
Antibody FormationMajor topic
B-LymphocytesMajor topic
H-2 AntigensMajor topic
Lymphocyte ActivationMajor topic
Lymphocyte CooperationMajor topic
MacrophagesMajor topic
T-LymphocytesMajor topic
Animals
Chromosome Mapping
Erythrocytes
Genetic Linkage
Heterozygote
Immunologic Memory
Immunosuppression Therapy
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.

References19

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

OrderPMIDTitleJournalYearIn PapersSource
114,037,719Graft versus host reactions. Their natural history, and applicability as tools of research.Prog Allergy1962https://conductscience.org/library/papers/14037719PubMed
2233,906Independent populations of primed F1 guinea pig T lymphocytes respond to antigen-pulsed parental peritoneal exudate cells.J Exp Med1977https://conductscience.org/library/papers/233906PubMed
370,357In vitro secondary mixed leukocyte reaction (MLR). II. Interaction MLR determinants expressed by F1 cells.Eur J Immunol1977https://conductscience.org/library/papers/70357PubMed
475,242
The role of H-2 linked genes in helper T-cell function. II. Isolation on antigen-pulsed macrophages of two separate populations of F1 helper T cells each specific for antigen and one set of parental H-2 products.
J Exp Med1978https://conductscience.org/library/papers/75242PubMed
5302,180The significance of T-B collaboration across haplotype barriers.Cold Spring Harb Symp Quant Biol1977https://conductscience.org/library/papers/302180PubMed
61,086,883Allogeneic carrier-specific enhancement of hapten-specific secondary B-cell responses.J Exp Med1976https://conductscience.org/library/papers/1086883PubMed
71,027,410The origin and significance of macrophages in thoracic duct lymph.Aust J Exp Biol Med Sci1976https://conductscience.org/library/papers/1027410PubMed
81,085,419Helper T cells recognise antigen and macrophage surface components simultaneously.Nature1976https://conductscience.org/library/papers/1085419PubMed
94,122,709
Cell interactions between histoincompatible T and B lymphocytes. II. Failure of physiologic cooperative interactions between T and B lymphocytes from allogeneic donor strains in humoral response to hapten-protein conjugates.
J Exp Med1973https://conductscience.org/library/papers/4122709PubMed
1058,463Specificity of virus-immune effector T cells for H-2K or H-2D compatible interactions: implications for H-antigen diversity.Transplant Rev1976https://conductscience.org/library/papers/58463PubMed

1 to 10 of 19

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Cited by57

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 203 citations.

PMIDTitleJournalYearIn PapersSource
35,130,112CITEMOXMBD: A flexible single-cell multimodal omics analysis framework to reveal the heterogeneity of immune cells.RNA Biol2022https://conductscience.org/library/papers/35130112PubMed
33,571,241In silico analysis suggests less effective MHC-II presentation of SARS-CoV-2 RBM peptides: Implication for neutralizing antibody responses.PLoS One2021https://conductscience.org/library/papers/33571241PubMed
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
8,642,265Bone marrow-derived cells fail to induce positive selection in thymus reaggregation cultures.J Exp Med1996https://conductscience.org/library/papers/8642265PubMed
8,294,858Immunoglobulin signal transduction guides the specificity of B cell-T cell interactions and is blocked in tolerant self-reactive B cells.J Exp Med1994https://conductscience.org/library/papers/8294858PubMed
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
7,020,898Surface receptors on lymphoreticular cells: sensory devices for host recognition of foreign antigens and neoplasia.Can Med Assoc J1980https://conductscience.org/library/papers/7020898PubMed
6,984,188B-cell growth factor: distinction from T-cell growth factor and B-cell maturation factor.Proc Natl Acad Sci U S A1982https://conductscience.org/library/papers/6984188PubMed
6,979,046Dissociation of two signals required for activation of resting B cells.Proc Natl Acad Sci U S A1982https://conductscience.org/library/papers/6979046PubMed

1 to 10 of 57

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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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