Literature DB >> 2697914

Dendritic cells in contact sensitivity.

S C Knight1.   

Abstract

Bone-marrow-derived DC, passing through the skin or residing there as LC, acquire antigen following epicutaneous exposure to contact sensitizer. They move as veiled cells in the afferent lymphatics and migrate to draining lymph nodes, where they become interdigitating cells of the paracortex. Here they initiate T-cell responses; the cytotoxic T cells and antibody formation which develop may be able to target on DC as well as other antigen-bearing cells, so producing feed-back mechanisms to switch off immune responses. Additional features include a systemic effect which leads to movement of DC without antigen into lymph nodes. What are the signals leading to this movement and what is its significance? There is evidence for synergy between directly haptenated DC and DC not directly acquiring antigen. How does this occur and how important is this effect in ensuring the potency of DC in presenting contact sensitizer to T cells? What is the importance of antigen processing by LC? Finally, dendriform cells which may be of T-cell origin are also present in the skin. What is their role in modulating the development of contact sensitivity?

Mesh:

Year:  1989        PMID: 2697914     DOI: 10.1016/0923-2494(89)90053-9

Source DB:  PubMed          Journal:  Res Immunol        ISSN: 0923-2494


  1 in total

1.  Tbet and IL-36γ cooperate in therapeutic DC-mediated promotion of ectopic lymphoid organogenesis in the tumor microenvironment.

Authors:  Aliyah M Weinstein; Lu Chen; Emily A Brzana; Prashanti R Patil; Jennifer L Taylor; Kellsye L Fabian; Callen T Wallace; Sabrina D Jones; Simon C Watkins; Binfeng Lu; David F Stroncek; Timothy L Denning; Yang-Xin Fu; Peter A Cohen; Walter J Storkus
Journal:  Oncoimmunology       Date:  2017-04-28       Impact factor: 8.110

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.