PMID- 8760789 OWN - NLM STAT- MEDLINE DCOM- 19960923 LR - 20190508 IS - 0022-1007 (Print) IS - 1540-9538 (Electronic) IS - 0022-1007 (Linking) VI - 184 IP - 2 DP - 1996 Aug 1 TI - Histamine selectively enhances human immunoglobulin E (IgE) and IgG4 production induced by anti-CD58 monoclonal antibody. PG - 357-64 AB - We studied the effects of histamine on human immunoglobulin (IgE) and IgG4 production. Histamine selectively enhanced IgE and IgG4 production in purified surface IgE and IgG4 negative (sIgE-sIgG4-) B cells from normal donors stimulated with interleukin (IL)-4 plus anti-CD58 or IL-13 plus anti-CD58 monoclonal antibody (mAb) without affecting production of IgG1, IgG2, IgG3, IgM, IgA1, or IgA2. In cultures with IL-4 plus anti-CD58 mAb, histamine-induced enhancement of IgE and IgG4 production was specifically blocked by thioperamide (H3 receptor antagonist), and was inhibited by anti-IL-10 antibody (Ab). In contrast, in cultures with IL-13 plus anti-CD58 mAb, histamine-induced enhancement was blocked by dimaprit (H1 receptor antagonist), and was inhibited by anti-IL-6 mAb. Histamine also enhanced IgE and IgG4 production by in vivo-generated sIgE+ and sIgG4+ B cells, respectively, from atopic patients; enhancement was blocked by dimaprit and thioperamide, and was inhibited by anti-IL-6 mAb and anti-IL-10 Ab. In sIgE-sIgG4- B cells, IL-4 plus anti-CD58 mAb induced IL-10 production and IL-10 receptor expression, whereas IL-13 plus anti-CD58 mAb induced IL-6 production and IL-6 receptor expression. Histamine increased IL-10 and IL-6 production without affecting IL-10 and IL-6 receptor expression, in cultures with IL-4 plus anti-CD58 mAb and with IL-13 plus anti-CD58 mAb, respectively, which was blocked by thioperamide and dimaprit, respectively. In contrast, sIgE+ and sIgG4+ B cells spontaneously produced both IL-6 and IL-10 and constitutively expressed IL-6 and IL-10 receptors, and histamine increased IL-6 and IL-10 production without affecting IL-6 or IL-10 receptor expression, which was blocked by thioperamide and dimaprit. These results indicate that histamine enhanced IgE and IgG4 production by increasing endogenous IL-6 and IL-10 production via H1 and H3 receptors, respectively. FAU - Kimata, H AU - Kimata H AD - Department of Pediatrics, Unitika Central Hospital, Kyoto, Japan. FAU - Fujimoto, M AU - Fujimoto M FAU - Ishioka, C AU - Ishioka C FAU - Yoshida, A AU - Yoshida A LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Exp Med JT - The Journal of experimental medicine JID - 2985109R RN - 0 (Antibodies, Monoclonal) RN - 0 (CD58 Antigens) RN - 0 (Immunoglobulin G) RN - 0 (Interleukin-13) RN - 0 (Interleukin-6) RN - 0 (Receptors, Histamine H1) RN - 0 (Receptors, Histamine H2) RN - 130068-27-8 (Interleukin-10) RN - 37341-29-0 (Immunoglobulin E) RN - 820484N8I3 (Histamine) SB - IM MH - Antibodies, Monoclonal MH - B-Lymphocyte Subsets/*metabolism MH - CD58 Antigens/*physiology MH - Cells, Cultured MH - Histamine/*administration & dosage MH - Humans MH - Immunoglobulin E/*biosynthesis MH - Immunoglobulin G/*biosynthesis MH - Interleukin-10/metabolism MH - Interleukin-13/administration & dosage MH - Interleukin-6/metabolism MH - Palatine Tonsil/cytology MH - Receptors, Histamine H1/metabolism MH - Receptors, Histamine H2/metabolism PMC - PMC2192716 EDAT- 1996/08/01 00:00 MHDA- 1996/08/01 00:01 PMCR- 1997/02/01 CRDT- 1996/08/01 00:00 PHST- 1996/08/01 00:00 [pubmed] PHST- 1996/08/01 00:01 [medline] PHST- 1996/08/01 00:00 [entrez] PHST- 1997/02/01 00:00 [pmc-release] AID - 96343846 [pii] AID - 10.1084/jem.184.2.357 [doi] PST - ppublish SO - J Exp Med. 1996 Aug 1;184(2):357-64. doi: 10.1084/jem.184.2.357.