scispace - formally typeset
B

B Benacerraf

Researcher at Albert Einstein College of Medicine

Publications -  89
Citations -  4068

B Benacerraf is an academic researcher from Albert Einstein College of Medicine. The author has contributed to research in topics: Antigen & T cell. The author has an hindex of 36, co-authored 89 publications receiving 4053 citations. Previous affiliations of B Benacerraf include Thomas Jefferson University.

Papers
More filters
Journal ArticleDOI

Cell interactions between histoincompatible T and B lymphocytes. VII. Cooperative responses between lymphocytes are controlled by genes in the I region of the H-2 complex

TL;DR: The results of this study provide compelling evidence for the existence of the gene or genes controlling optimal T-B-cell cooperative interactions in the designated I region of the H-2 gene complex.
Journal ArticleDOI

CELL INTERACTIONS BETWEEN HISTOINCOMPATIBLE T AND B LYMPHOCYTES : IV. INVOLVEMENT OF THE IMMUNE RESPONSE (Ir) GENE IN THE CONTROL OF LYMPHOCYTE INTERACTIONS IN RESPONSES CONTROLLED BY THE GENE

TL;DR: It is suggested that the gene(s) that conditions the capability for physiologic T-B cell cooperation must be shared in common by the respective cell types, and suggest, furthermore, that this gene (or genes) belongs to the major histocompatibility system of the mouse.
Journal ArticleDOI

Antigen- and receptor-driven regulatory mechanisms. IV. Idiotype-bearing I-J + suppressor T cell factors induce second-order suppressor T cells which express anti-idiotypic receptors

TL;DR: Data indicate that antigen elicits the production of a soluble T cell product bearing both variable portion of the Ig heavy chain (VH) and I-J subregion-coded determinants which serves to communicate between T cell subsets to establish an idiotype- anti-idiotype regulatory pathway.
Journal Article

Analysis of MHC class II presentation of particulate antigens of B lymphocytes.

TL;DR: It is found that B lymphoblastoid cell lines and LPS-activated B lymphocytes can present particulate Ag up to 10(5)-fold more efficiently compared with soluble Ag and that while Ag beads are bound to the cell surface, they are internalized only rarely, suggesting there may be both surface and intracellular pathways for the presentation of particulates Ags by B cells.
Journal ArticleDOI

Shared idiotypic determinants on antibodies and T-cell-derived suppressor factor specific for the random terpolymer L-glutamic acid60-L-alanine30-L-tyrosine10.

TL;DR: Evidence is provided suggesting a sharing of V region structures between B- cell antibody and T- cell suppressor factor specific for an antigen (GAT) under Ir gene control, in agreement with earlier studies on T and B-cell alloreceptors, T-cell helper factors, and T andB-cell receptors for conventional antigens.