# Inhibition of antibody production in vivo by pre-stimulation of toll-like receptor 4 before antigen priming is caused by defective B-cell priming and not impairment in antigen presentation > Rachmawati N.M. URL kanonis: https://discover.unhas.ac.id/publications/pub_scopus_84873802103 Jurnal / Konferensi: International Immunology Tahun terbit: 2013 DOI: https://doi.org/10.1093/intimm/dxs096 ISSN: 09538178 Kuartil SJR: Q1 Citations: 7 ## Authors - Rachmawati N.M. ## Abstract Stimulation of Toll-like receptor 4 (TLR4) induces not only innate but also adaptive immune responses, and has been suggested to exert adjuvant effects. Additional to such positive effects, pre-stimulation of TLR4 induces endotoxin tolerance where animals are unresponsive to subsequent lethal challenges with lipopolysaccharide (LPS). We examined the effects of pre-stimulation of TLR4 using an agonistic anti-TLR4 mAb (UT12) on antibody production in vivo. Pre-injection of UT12 prior to both primary and secondary immunization completely inhibited antigen-specific antibody responses. Cellular analysis revealed that the inhibition was not due to impairment of T-cell activation. Accordingly, T-helper activities in UT12 pre-injected mice were not impaired. In contrast, B-cell priming was defective in UT12 pre-injected mice. The observation that the expression of activation markers such as CD69 and CD86 on B cells was blocked by UT12 pre-injection supports this. Interestingly, UT12 pre-injection only showed inhibitory effects at the primary and not the secondary immunization. These results provide important information concerning the regulatory mechanisms of antibody production, especially in endotoxin-tolerant states. ## Keywords - Priming (agriculture) - TLR4 - Antigen - Stimulation - Immunology - CD86 - In vivo - Immune system - Antibody - Lipopolysaccharide - Toll-like receptor - T cell - Adjuvant - Biology - Receptor - Immune tolerance - Innate immune system - Endocrinology - Biochemistry - Germination - Botany - Biotechnology --- Sumber: Discover Unhas — RIMS Universitas Hasanuddin. Saat mengutip, gunakan DOI bila tersedia atau URL kanonis di atas.