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Selective M1 macrophage polarization in granulomapositive and granuloma-negative Crohn's disease, in comparison to intestinal tuberculosis.

Authors :
Das, Prasenjit
Rampal, Ritika
Udinia, Sonakshi
Kumar, Tarun
Pilli, Sucharita
Wari, Nahid
Ahmed, Imtiaz Khan
Kedia, Saurabh
Gupta, Siddhartha Datta
Kumar, Dhiraj
Ahuja, Vineet
Source :
Intestinal Research. Jul2018, Vol. 16 Issue 3, p426-435. 10p.
Publication Year :
2018

Abstract

Background/Aims: Classical M1 macrophage activation exhibits an inflammatory phenotype while alternative M2 macrophage activation exhibits an anti-inflammatory phenotype. We aimed to determine whether there are discriminant patterns of macrophage polarization in Crohn's disease (CD) and intestinal tuberculosis (iTB). Methods: Colonic mucosal biopsies from 29 patients with iTB, 50 with CD, and 19 controls were examined. Dual colored immunohistochemistry was performed for iNOS/CD68 (an M1ϕ marker) and CD163/CD68 (an M2ϕ marker), and the ratio of M1ϕ to M2ϕ was assessed. To establish the innate nature of macrophage polarization, we analyzed the extent of mitochondrial depolarization, a key marker of inflammatory responses, in monocyte-derived macrophages obtained from CD and iTB patients, following interferon-γ treatment. Results: M1ϕ polarization was more prominent in CD biopsies (P =0.002) than in iTB (P =0.2) and control biopsies. In granuloma-positive biopsies, including those in CD, M1ϕ predominance was significant (P =0.001). In iTB, the densities of M1ϕ did not differ between granuloma-positive and granuloma-negative biopsies (P =0.1). Interestingly, higher M1ϕ polarization in CD biopsies correlated with high inflammatory response exhibited by peripheral blood-derived monocytes from these patients. Conclusions: Proinflammatory M1ϕ polarization was more common in colonic mucosa of CD patients, especially in the presence of mucosal granulomas. Further characterization of the innate immune system could help in clarifying the pathology of iTB and CD. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
15989100
Volume :
16
Issue :
3
Database :
Academic Search Index
Journal :
Intestinal Research
Publication Type :
Academic Journal
Accession number :
130941184
Full Text :
https://doi.org/10.5217/ir.2018.16.3.426