| Literature DB >> 1165105 |
Abstract
Mice primed to human serum albumin (HSA) by means of an HSA--sheep red cell conjugate, developed a high level of memory to HSA, with little concomitant antibody production ('pure priming'). The proportion of HSA-specific antigen-binding cells was determined in the spleens of the primed mice by means of a rosette technique, using an HSA-donkey red cell conjugate. The specificity of the rosette-forming cells (RFC) was confirmed by the ability of soluble HSA to inhibit rosette formation. Highly enriched rosette suspensions (up to 40-fold enrichment) were prepared by bovine serum albumin density gradient centrifugation. The enriched suspensions could transfer adoptively memory to HSA, whereas the rosette-depleted fractions were totally inactive. It was thus confirmed that memory cells are included in the antigen-binding cells. A detectable level of memory could be transferred with 3000 rosettes. RFC similarly isolated from spleens of non-primed mice could also transfer a low level of responsiveness to HSA, but only when large numbers (70,000) were injected, together with primed, RFC-depleted spleen cells.Entities:
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Year: 1975 PMID: 1165105 PMCID: PMC1445969
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397