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Paper · 1348366

Memory cell generation ablated by soluble protein antigen by means of effects on T- and B-lymphocyte compartments.

Karvelas M and 1 other. Proc Natl Acad Sci U S A, 1992. Cited by 22 papers, by iCite.

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ConductScience Library. Memory cell generation ablated by soluble protein antigen by means of effects on T- and B-lymphocyte compartments. Papers, record 1348366. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/1348366

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Paper

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

Title
Memory cell generation ablated by soluble protein antigen by means of effects on T- and B-lymphocyte compartments.
PubMed
Journal
Proc Natl Acad Sci U S A
PubMed
Year
1992
PubMed
Publication types
Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
PubMed
Citations, by iCite
22
iCite
Relative citation ratio, by iCite
0.34
iCite
Revised in PubMed
2019-05-01
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Karvelas MM
2Nossal GJG J

Source PubMed

Topics15

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

MeSH termMajor
AntigensMajor topic
B-LymphocytesMajor topic
Immune ToleranceMajor topic
Immunologic MemoryMajor topic
T-LymphocytesMajor topic
Animals
CD4-Positive T-Lymphocytes
Immunization, Passive
Lymphocyte Activation
Mice
Mice, Inbred C57BL
Serum Albumin
Solubility
Specific Pathogen-Free Organisms
Spleen

Source PubMed

Grants1

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.

Grant, as the record writes itAgencyCountryNIH projectStated by
AI-03958NIAID NIH HHSUnited StatesR01AI003958PubMed and NIH

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.

References32

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

OrderPMIDTitleJournalYearIn PapersSource
12,079,328Transgenic mice as an in vivo model for self-reactivity.Immunol Rev1990https://conductscience.org/library/papers/2079328PubMed
22,014,051Molecular characterization of single memory B cells.Nature1991https://conductscience.org/library/papers/2014051PubMed
32,783,762Clonal deletion of B lymphocytes in a transgenic mouse bearing anti-MHC class I antibody genes.Nature1989https://conductscience.org/library/papers/2783762PubMed
44,192,271Cellular sites of immunologic unresponsiveness.Proc Natl Acad Sci U S A1970https://conductscience.org/library/papers/4192271PubMed
56,211,808Suppressor cells in transplantation tolerance. I. Analysis of the suppressor status of neonatally and adoptively tolerized rats.Transplantation1982https://conductscience.org/library/papers/6211808PubMed
66,367,046Biological activity of recombinant human interleukin-2 produced in Escherichia coli.Science1984https://conductscience.org/library/papers/6367046PubMed
72,823,259Isolation and characterization of lymphokine cDNA clones encoding mouse and human IgA-enhancing factor and eosinophil colony-stimulating factor activities: relationship to interleukin 5.Proc Natl Acad Sci U S A1987https://conductscience.org/library/papers/2823259PubMed
83,161,079A role for suppressor T cells in induction of self-tolerance.Proc Natl Acad Sci U S A1985https://conductscience.org/library/papers/3161079PubMed
93,889,907A high-efficiency cloning system for single hapten-specific B lymphocytes that is suitable for assay of putative growth and differentiation factors.Proc Natl Acad Sci U S A1985https://conductscience.org/library/papers/3889907PubMed
1057,094Single cell studies on the antibody-forming potential of fractionated, hapten-specific B lymphocytes.Immunology1976https://conductscience.org/library/papers/57094PubMed

Cited by5

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 22 citations.

PMIDTitleJournalYearIn PapersSource
8,879,198A disease-related rheumatoid factor autoantibody is not tolerized in a normal mouse: implications for the origins of autoantibodies in autoimmune disease.J Exp Med1996https://conductscience.org/library/papers/8879198PubMed
8,464,928Soluble antigen profoundly reduces memory B-cell numbers even when given after challenge immunization.Proc Natl Acad Sci U S A1993https://conductscience.org/library/papers/8464928PubMed
8,356,062Peripheral T-cell tolerance induced in naive and primed mice by subcutaneous injection of peptides from the major cat allergen Fel d I.Proc Natl Acad Sci U S A1993https://conductscience.org/library/papers/8356062PubMed
7,809,146Control of autoantibody affinity by selection against amino acid replacements in the complementarity-determining regions.Proc Natl Acad Sci U S A1994https://conductscience.org/library/papers/7809146PubMed
1,478,378Autoimmune tolerance and type 1 (insulin-dependent) diabetes mellitus.Diabetologia1992https://conductscience.org/library/papers/1478378PubMed

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
ALB213PubTator's text mininghttps://conductscience.org/library/genes/213

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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