4.6 Article

Hypochlorous Acid: A Natural Adjuvant That Facilitates Antigen Processing, Cross-Priming, and the Induction of Adaptive Immunity

Journal

JOURNAL OF IMMUNOLOGY
Volume 184, Issue 2, Pages 824-835

Publisher

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0902606

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Funding

  1. European Union [TEAM/2008-2/6]
  2. Jagiellonian University Medical College [K/ZDS/001008]
  3. Biotechnology and Biological Sciences Research Council Selective Chemical Intervention in Biological Systems initiative
  4. Medical Research Council [G9721629, G0900950, G9721629B, G0900950B] Funding Source: researchfish
  5. MRC [G0900950, G9721629] Funding Source: UKRI

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The production of hypochlorous acid (HOCl) is a characteristic of granulocyte activation, a hallmark of the early phase of innate immune responses. In this study, we show that, in addition to Its Well-established role as a microbicide, HOCl can act as a natural adjuvant of adaptive immunity. HOCl enhances the T cell responses to the model Ag OVA, facilitating the processing and presentation of this protein via the class H MHC pathway. HOCl modification also enhances cross-presentation of the tumor Ag tyrosinase-related protein 2 via class I MHC. The adjuvant effects of HOCl are independent of TLR signaling. The enhanced presentation of HOCl-modified OVA is mediated via modification of the N-linked carbohydrate side chain rather than formation of protein aldehydes or chloramines. HOCl-modified OVA is taken up more efficiently by APCs and is degraded more efficiently by proteinases. Atomic force microscopy demonstrated that enhanced uptake is mediated via specific receptor binding, one candidate for which is the scavenger receptor lectin-like oxidized low-density lipoprotein receptor, which shows enhanced binding to chlorinated OVA. A function of HOCl is therefore to target glycoprotein Ags to scavenger receptors on the APC surface. This additional mechanism linking innate and adaptive immunity suggests novel strategies to enhance immunity to vaccines. The Journal of Immunology, 2010, 184: 824-835.

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