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Paper6229596

Allosuppressor and allohelper T cells in acute and chronic graft-vs-host disease. V. F1 mice with secondary chronic GVHD contain F1-reactive allohelper but no allosuppressor T cells.

Pals ST and 2 others. J Exp Med, 1984. Cited by 40 papers, by iCite.

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ConductScience Library. Allosuppressor and allohelper T cells in acute and chronic graft-vs-host disease. V. F1 mice with secondary chronic GVHD contain F1-reactive allohelper but no allosuppressor T cells. Papers, record 6229596. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/6229596

Paper

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

Title
Allosuppressor and allohelper T cells in acute and chronic graft-vs-host disease. V. F1 mice with secondary chronic GVHD contain F1-reactive allohelper but no allosuppressor T cells.
PubMed
Journal
J Exp Med
PubMed
Year
1984
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't
PubMed
Citations, by iCite
40
iCite
Relative citation ratio, by iCite
1.01
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
1Pals STS T
2Gleichmann HH
3Gleichmann EE

Source PubMed

Topics18

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

MeSH termMajor
Graft vs Host DiseaseMajor topic
T-Lymphocytes, Helper-InducerMajor topic
T-Lymphocytes, RegulatoryMajor topic
Acute Disease
Animals
Chronic Disease
Crosses, Genetic
Female
Hematopoiesis
Hematopoietic Stem Cells
Immune Tolerance
Immunization, Passive
Lymphoid Tissue
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Radiation Chimera
Spleen

Source PubMed

References34

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

OrderPMIDTitleJournalYearIn PapersSource
16,445,861Suppressive mechanisms involving sensitization and tolerance in contact allergy.Immunol Rev1980https://conductscience.org/library/papers/6445861PubMed
24,404,878Serologically defined and lymphocyte-defined components of the major histocompatibility complex in the mouse.J Exp Med1972https://conductscience.org/library/papers/4404878PubMed
37,410,851Models for the production of stable hematopoietic chimerism across major histocompatibility barriers in adults.J Immunol1980https://conductscience.org/library/papers/7410851PubMed
46,448,894Cell-mediated immunity to non-HLA antigens of the host by donor lymphocytes in patients with chronic graft-vs-host disease.J Immunol1980https://conductscience.org/library/papers/6448894PubMed
56,452,977Immune function in fully allogeneic mouse bone marrow chimeras.Clin Immunol Immunopathol1981https://conductscience.org/library/papers/6452977PubMed
66,166,716Self recognition in allogeneic radiation bone marrow chimeras. A radiation-resistant host element dictates the self specificity and immune response gene phenotype of T-helper cells.J Exp Med1981https://conductscience.org/library/papers/6166716PubMed
76,454,750
Capacity of genetically different T lymphocytes to induce lethal graft-versus-host disease correlates with their capacity to generate suppression but not with their capacity to generate anti-F1 killer cells. A non-H-2 locus determines the inability to induce lethal graft-versus-host disease.
J Exp Med1981https://conductscience.org/library/papers/6454750PubMed
87,021,693Improvement of the protein A plaque assay for immunoglobulin secreting cells by using immunoglobulin-depleted guinea pig serum as a source of complement.J Immunol Methods1981https://conductscience.org/library/papers/7021693PubMed
96,461,714
Allosuppressor and allohelper T cells in acute and chronic graft-vs-host disease. I. Alloreactive suppressor cells rather than killer T cells appear to be the decisive effector cells in lethal graft-vs.-host disease.
J Exp Med1982https://conductscience.org/library/papers/6461714PubMed
106,978,376
Diseases caused by reactions of T lymphocytes towards incompatible structures of the major histocompatibility complex. VI. Autoantibodies characteristic of systemic lupus erythematosus induced by abnormal T-B cell cooperation across I-E.
J Exp Med1982https://conductscience.org/library/papers/6978376PubMed
116,978,818A systemic lupus erythematosus (SLE)-like disease in mice induced by abnormal T-B cell cooperation. Preferential formation of autoantibodies characteristic of SLE.Eur J Immunol1982https://conductscience.org/library/papers/6978818PubMed
126,213,709Modulation of F1 cytotoxic potentials by GvHR: suppression of cytotoxic T cell responses of F1 mice correlates with F1 inability to resist the proliferation of GvHR-inducing parental T lymphocytes.J Immunol1982https://conductscience.org/library/papers/6213709PubMed
137,050,708Identification by HLA typing of intrauterine-derived maternal T cells in four patients with severe combined immunodeficiency.N Engl J Med1982https://conductscience.org/library/papers/7050708PubMed
144,266,664A major role for the Ir-1 region of the mouse H-2 complex in the mixed leukocyte reaction.Transplant Proc1973https://conductscience.org/library/papers/4266664PubMed
154,587,740A rapid method for the isolation of functional thymus-derived murine lymphocytes.Eur J Immunol1973https://conductscience.org/library/papers/4587740PubMed
164,151,282Cellular immunology and the pathogenesis of graft versus host reactions.Prog Allergy1971https://conductscience.org/library/papers/4151282PubMed
17124,761Association of immunity and tolerance to host H-2 determinants in irradiated F1 hybrid mice reconstituted with bone marrow cells from one parental strain.J Exp Med1975https://conductscience.org/library/papers/124761PubMed
1851,901Collaboration of histoincompatible T and B lymphocytes using cells from tetraparental bone marrow chimeras.J Exp Med1975https://conductscience.org/library/papers/51901PubMed
1914,213Suppressor T cells arising in mice undergoing a graft-vs-host response.J Immunol1977https://conductscience.org/library/papers/14213PubMed
2016,073The Ly phenotype of suppressor T cells arising in mice subjected to a graft-versus-host reaction.J Exp Med1977https://conductscience.org/library/papers/16073PubMed

See all 34 references

Cited by7

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 40 citations.

PMIDTitleJournalYearIn PapersSource
40,433,377Identification and validation of tissue-based gene biomarkers for acute intestinal graft-versus-host disease(AIGVHD).Front Immunol2025https://conductscience.org/library/papers/40433377PubMed
16,791,603Nephrotic syndrome in a child after umbilical-cord-blood transplantation.Pediatr Nephrol2006https://conductscience.org/library/papers/16791603PubMed
8,958,055Completely allogeneic spleen cells induced cytolytic neonatal tolerance to alloantigens, but failed to establish allo-helper interactions with host T cells.Immunology1996https://conductscience.org/library/papers/8958055PubMed
2,957,456Regulation of autoimmunity and donor cell engraftment by recipient Lyt-2+ cells during the graft-versus-host reaction.J Exp Med1987https://conductscience.org/library/papers/2957456PubMed
2,873,640Bone marrow transplantation: the genetic and cellular basis of resistance to engraftment and acute graft-versus-host disease.Surv Immunol Res1985https://conductscience.org/library/papers/2873640PubMed
2,531,761Intestinal graft-versus-host disease is initiated by donor T cells distinct from classic cytotoxic T lymphocytes.J Clin Invest1989https://conductscience.org/library/papers/2531761PubMed
2,148,286Persistence of allospecific helper T cells is required for maintaining autoantibody formation in lupus-like graft-versus-host disease.Clin Exp Immunol1990https://conductscience.org/library/papers/2148286PubMed

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

None in this release

  • Grants
  • Trials
  • Comments and corrections
  • Genes
  • Drugs
  • Data

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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