Abstract
Mycobacteria in complete Freund's adjuvant (CFA) are an essential component of immunization protocols in a number of autoimmune disease animal models including experimental autoimmune encephalomyelitis and uveoretinitis (EAE and EAU, respectively). We determined the role in EAU of two C-type lectin receptors on myeloid cells that recognize and respond to mycobacteria. Using receptor-specific antibodies and knockout mice, we demonstrated for the first time that the macrophage mannose receptor delays disease development but does not affect severity. In contrast, dectin-1 is critically involved in the development of CFA-mediated EAU. Disease severity is reduced in dectin-1 knockout mice and antibody blockade of dectin-1 during the induction, but not the effector phase, prevents EAU development. Significantly, similar blockade of dectin-1 in vivo has no effect in non-CFA-mediated, spontaneously induced or adoptive transfer models of EAU. Thus dectin-1 plays a critical role in the ability of complete Freund's adjuvant to induce EAU in mice.
| Original language | English |
|---|---|
| Pages (from-to) | 398-406 |
| Number of pages | 9 |
| Journal | Molecular Immunology |
| Volume | 67 |
| Issue number | 2 |
| DOIs | |
| State | Published - 01 10 2015 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015.
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This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adjuvant
- Dectin-1
- Experimental autoimmune uveitis
- Macrophage mannose receptor
- Mycobacteria
- Pattern recognition receptor
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