1,25-Dihydroxy vitamin D sub(3) downregulates pro-inflammatory cytokine response in pulmonary tuberculosis

1,25-Dihydroxy vitamin D sub(3) [1,25(OH) sub(2)D sub(3)] is a potent immunomodulator and regulates various immune responses to Mycobacterium tuberculosis (Mtb). The present study aimed to understand the effect of 1,25(OH) sub(2)D sub(3) on pro-inflammatory cytokine response to Mtb antigen. Peripher...

Full description

Saved in:
Bibliographic Details
Published in:International immunopharmacology Vol. 23; no. 1; pp. 148 - 152
Main Authors: Harishankar, M, Afsal, K, Banurekha, V V, Meenakshi, N, Selvaraj, P
Format: Journal Article
Language:English
Published: 01-11-2014
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:1,25-Dihydroxy vitamin D sub(3) [1,25(OH) sub(2)D sub(3)] is a potent immunomodulator and regulates various immune responses to Mycobacterium tuberculosis (Mtb). The present study aimed to understand the effect of 1,25(OH) sub(2)D sub(3) on pro-inflammatory cytokine response to Mtb antigen. Peripheral blood mononuclear cells from 42 healthy controls (HCs) and 42 pulmonary tuberculosis (PTB) patients were cultured with culture filtrate antigen (CFA) of Mtb with and without 1,25(OH) sub(2)D sub(3) at 10 super(- 7) M concentration for 72 h. The levels of IL-1 alpha , IL-1 beta , TNF- alpha , TNF- beta , IL-17 and IL-23 were estimated in the culture supernatants by ELISA. 1,25(OH) sub(2)D sub(3) significantly suppressed all the CFA induced pro-inflammatory cytokines (p < 0.05) studied except IL-1 beta in both HCs and PTB patients. Among the PTB patients, the observed suppression was visible both in patients with and without cavitary tuberculosis. The present study results suggest that 1,25(OH) sub(2)D sub(3) downregulates the production of pro-inflammatory cytokines and may control the exacerbated inflammatory response that may protect the host from excessive tissue damage at the site of infection.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
content type line 23
ObjectType-Feature-2
ISSN:1567-5769
DOI:10.1016/j.intimp.2014.08.021