LL-37 immunomodulatory activity during Mycobacterium tuberculosis infection in macrophages.

Abstract:

:Tuberculosis is one of the most important infectious diseases worldwide. The susceptibility to this disease depends to a great extent on the innate immune response against mycobacteria. Host defense peptides (HDP) are one of the first barriers to counteract infection. Cathelicidin (LL-37) is an HDP that has many immunomodulatory effects besides its weak antimicrobial activity. Despite advances in the study of the innate immune response in tuberculosis, the immunological role of LL-37 during M. tuberculosis infection has not been clarified. Monocyte-derived macrophages were infected with M. tuberculosis strain H37Rv and then treated with 1, 5, or 15 μg/ml of exogenous LL-37 for 4, 8, and 24 h. Exogenous LL-37 decreased tumor necrosis factor alpha (TNF-α) and interleukin-17 (IL-17) while inducing anti-inflammatory IL-10 and transforming growth factor β (TGF-β) production. Interestingly, the decreased production of anti-inflammatory cytokines did not reduce antimycobacterial activity. These results are consistent with the concept that LL-37 can modulate the expression of cytokines during mycobacterial infection and this activity was independent of the P2X7 receptor. Thus, LL-37 modulates the response of macrophages during infection, controlling the expression of proinflammatory and anti-inflammatory cytokines.

journal_name

Infect Immun

journal_title

Infection and immunity

authors

Torres-Juarez F,Cardenas-Vargas A,Montoya-Rosales A,González-Curiel I,Garcia-Hernandez MH,Enciso-Moreno JA,Hancock RE,Rivas-Santiago B

doi

10.1128/IAI.00936-15

subject

Has Abstract

pub_date

2015-12-01 00:00:00

pages

4495-503

issue

12

eissn

0019-9567

issn

1098-5522

pii

IAI.00936-15

journal_volume

83

pub_type

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