Enhanced Mycobacterial Antigen-Induced Pro-Inflammatory Cytokine Production in Lymph Node Tuberculosis.

Authors:
Gokul Raj Kathamuthu
Gokul Raj Kathamuthu
National Institutes of Health-National Institute for Research in Tuberculosis-International Center for Excellence in Research
Kadar Moideen
Kadar Moideen
National Institutes of Health-NIRT-International Center for Excellence in Research
Rathinam Sridhar
Rathinam Sridhar
Government Stanley Medical Hospital
Chennai | India
Dhanaraj Baskaran
Dhanaraj Baskaran
National Institute for Research in Tuberculosis
Chennai | India
Subash Babu
Subash Babu
National Institutes of Health-NIRT-International Center for Excellence in Research
Bethesda | United States

Am J Trop Med Hyg 2019 Apr 15. Epub 2019 Apr 15.

Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, Maryland.

Lymph node tuberculosis (LNTB) is characterized by the enhanced baseline and antigen-specific production of type 1/17 cytokines and reduced baseline and antigen-specific production of interleukin (IL)-1β and IL-18 at the site of infection when compared with peripheral blood. However, the cytokine profile in the lymph nodes (LNs) of culture-positive LNTB (LNTB+) and negative LNTB (LNTB-) has not been examined. To address this, we have examined the baseline and mycobacterial antigen-stimulated cytokine levels of type 1 (interferon gamma [IFNγ], tumor necrosis factor alpha [TNFα], IL-2), type 2 (IL-4, IL-5, and IL-13), type 17 (IL-17A, IL-17F, and IL-22), pro-inflammatory (IL-1α, IL-1β, IL-18, and GM-CSF), and regulatory cytokines (IL-10, TGFβ) in the LN culture supernatants of LNTB+ and LNTB- individuals. We have observed significantly enhanced baseline levels of IL-13 and IL-10 and significantly reduced baseline levels of IL-4 and GM-CSF in LNTB+ individuals compared with LNTB- individuals. By contrast, we have observed significantly enhanced levels of type 1 (IFNγ, TNFα, and IL-2), type 17 (IL-17F and IL-22), and pro-inflammatory (IL-1α and GM-CSF) cytokines and significantly reduced levels of TGFβ in response to purified protein derivative, early secreted antigen-6, and culture filtrate protein-10 antigens in LNTB+ compared with LNTB- individuals. On phorbol 12-myristate 13-acetate/ionomycin stimulation, no significant difference was observed for any of the cytokines examined. Thus, our study revealed several interesting differences in the cytokine profiles of mycobacterial antigen-stimulated LN cultures in LNTB+ and LNTB- individuals. Therefore, we suggest the presence of mycobacteria plays a significant role in driving the cytokine response at the site of infection in LNTB.

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Source
http://dx.doi.org/10.4269/ajtmh.18-0834DOI Listing
April 2019
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