Document 3205 DOCN M94A3205 TI Primary antibody response of human lymphocytes from SCID-hu mice injected with HIV1 peptides. DT 9412 AU Touraine JL; Chargui J; Desgranges C; Transplantation & Clinical Immunology Unit, INSERM U80, Lyon,; France. SO Int Conf AIDS. 1994 Aug 7-12;10(1):129 (abstract no. PA0135). Unique Identifier : AIDSLINE ICA10/94369370 AB OBJECTIVE: Severe combined immunodeficiency (SCID) mice can be transplanted with human lymphocytes (hu-PBL-SCID) or with human fetal liver, thymus and bone fragments (SCID-hu), thus providing a model for the study of HIV infection. This model has been used to investigate in vivo anti-HIV antibody response by human cells from such mice. METHODS: Hu-PBL-SCID and SCID-hu mice were injected with a variety of peptides from gp41 and antibodies were repeatedly checked by ELISA in mouse sera. RESULTS: Primary then secondary responses were shown to occur in SCID-hu mice, with 225 mg/l of human IgM and 300-1860 mg/l of human IgG. The antibody response was demonstrated to be primary in nature, particularly since the human cells derived from naive, fetal precursor cells. When hu-PBL-SCID mice received HIV peptides, only IgM anti-HIV antibodies were produced (372-424 mg/l); the switch to IgG antibodies did not occur, possibly due to the lack of human antigen-presenting cells (APC) in these mice injected with non-adherent PBL, in contrast with the normal development of APC from human stem cells in SCID-hu mice. DISCUSSION AND CONCLUSION: Such humanized mice therefore lend themselves to anti-HIV antibody production, including human monoclonal antibodies to HIV and they possibly will also contribute to preclinical evaluation of HIV candidate vaccines. DE Animal *Antibody Formation Antigen-Presenting Cells/IMMUNOLOGY Comparative Study Enzyme-Linked Immunosorbent Assay Human HIV Antibodies/*BIOSYNTHESIS/BLOOD HIV Envelope Protein gp41/*IMMUNOLOGY IgG/BIOSYNTHESIS IgM/BIOSYNTHESIS/BLOOD *Lymphocyte Transfusion Mice Mice, SCID Peptide Fragments/IMMUNOLOGY MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).