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Paper62670

Expression of new idiotypes following neonatal idiotypic suppression of a dominant clone.

Augustin A and 1 other. Eur J Immunol, 1976. Cited by 96 papers, by iCite.

11 sourcespapers-2026-11-12-0.1.0

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ConductScience Library. Expression of new idiotypes following neonatal idiotypic suppression of a dominant clone. Papers, record 62670. Release papers-2026-11-12-0.1.0, 12 Nov 2026. https://conductscience.org/library/papers/62670

Paper

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

Title
Expression of new idiotypes following neonatal idiotypic suppression of a dominant clone.
PubMed
Journal
Eur J Immunol
PubMed
Year
1976
PubMed
Publication types
Journal Article
PubMed
Citations, by iCite
96
iCite
Relative citation ratio, by iCite
2.09
iCite
Revised in PubMed
2021-12-03
PubMed

Authors2

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

OrderAuthorForenameKindORCID iD
1Augustin AA
2Cosenza HH

Source PubMed

Topics13

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

MeSH termMajor
Animals, NewbornMajor topic
CholineMajor topic
Immunoglobulin AllotypesMajor topic
Immunosuppression TherapyMajor topic
PhosphorylcholineMajor topic
Age Factors
Animals
Antibodies, Anti-Idiotypic
Antigen-Antibody Reactions
Epitopes
Mice
Mice, Inbred BALB C
Myeloma Proteins

Source PubMed

Cited by17

The papers in our copy of PubMed whose reference list names this one, newest first. iCite, which reads more sources, counts 96 citations.

PMIDTitleJournalYearIn PapersSource
32,477,339Relevance of the Materno-Fetal Interface for the Induction of Antigen-Specific Immune Tolerance.Front Immunol2020https://conductscience.org/library/papers/32477339PubMed
9,989,978Neonatal idiotypic exposure alters subsequent cytokine, pathology, and survival patterns in experimental Schistosoma mansoni infections.J Exp Med1999https://conductscience.org/library/papers/9989978PubMed
9,393,802Oligoclonality of serum immunoglobulin G antibody responses to Streptococcus pneumoniae capsular polysaccharide serotypes 6B, 14, and 23F.Infect Immun1997https://conductscience.org/library/papers/9393802PubMed
8,943,710Autologous anti-idiotypic antibody response is regulated by the level of circulating complementary idiotype.Immunology1996https://conductscience.org/library/papers/8943710PubMed
7,252,411Antiphosphocholine antibodies found in normal mouse serum are protective against intravenous infection with type 3 streptococcus pneumoniae.J Exp Med1981https://conductscience.org/library/papers/7252411PubMed
6,972,994Generation of idiotype-specific T cell help through network perturbation.J Exp Med1981https://conductscience.org/library/papers/6972994PubMed
6,377,539Suppression of autoimmune diseases with anti-idiotypic antibodies: murine lupus nephritis as a model.Springer Semin Immunopathol1984https://conductscience.org/library/papers/6377539PubMed
6,222,133Induction of idiotype-specific suppressor T cells with antigen/antibody complexes.J Exp Med1983https://conductscience.org/library/papers/6222133PubMed
6,213,731Immunoglobulin idiotopes expressed by T cells. I. Expression of distinct idiotopes detected by monoclonal antibodies on antigen-specific suppressor T cells.J Exp Med1982https://conductscience.org/library/papers/6213731PubMed
6,163,071Autoregulation of immune responses via idiotype network interactions.Microbiol Rev1980https://conductscience.org/library/papers/6163071PubMed
3,081,440Isoelectric focusing spectra of anti-bacterial alpha-amylase antibody unique for antigen-induced suppression.Immunology1986https://conductscience.org/library/papers/3081440PubMed
2,580,040Cellular basis for neonatally induced T-suppressor activity. Primary B cell maturation is blocked by suppressor-helper interactions restricted by loci on chromosome 12.J Exp Med1985https://conductscience.org/library/papers/2580040PubMed
702,066Alteration of clonal profile. I. Effect of sublethal irradiation on the responses to phosphorylcholine in BALB/c mice.J Exp Med1978https://conductscience.org/library/papers/702066PubMed
410,029Potentiation of a primary in vivo antibody response by alloantisera against gene products of the I region of the H-2 complex.Proc Natl Acad Sci U S A1977https://conductscience.org/library/papers/410029PubMed
309,912Anti-idiotype induced regulation of helper cell function for the response to phosphorylcholine in adult BALB/c mice.J Exp Med1978https://conductscience.org/library/papers/309912PubMed
306,109Clonal dominance: loss and restoration in adoptive transfer.Proc Natl Acad Sci U S A1978https://conductscience.org/library/papers/306109PubMed
78,956Simultaneous complementary idiotypic responses: absence of reciprocal regulation.J Exp Med1978https://conductscience.org/library/papers/78956PubMed

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
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  • Comments and corrections
  • References
  • 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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