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Journal of Clinical Immunology and Allergy

ISSN: 2471-304X

16

th

EuroSciCon Conference on

Immunology

M a r c h 1 1 - 1 2 , 2 0 1 9

Am s t e r d a m , N e t h e r l a n d s

Immunology 2019

Ceren Ciraci et al., J Clin Immunol Allergy 2019, Volume:5

DOI: 10.21767/2471-304X-C1-009

T

he NLR family is a relatively newly discovered family of Pattern recognition

receptors whose functions have been examined almost exclusively in

innate immunity. There are 22 known members of the NLR family in humans,

four of which form a multiprotein complex called the inflammasome complex.

Besides inflammasome complex formation, the NLR family members have

been demonstrated to have associations with several diseases such as

artherosclerosis, type II diabetes, obesity, Alzheimer’s disease, gout and

bacterial, viral and parasite infections. One of the members of the NLR family,

NOD-like Receptor 11 (NLRP11) is expressed only in primates; however, its

cellular functions as well as the specific stimulant(s) that activate it are largely

unknown. To examine whether NLRP11 forms an inflammasome complex

and whether it has regulatory roles in shaping adaptive immune responses,

we investigated its potential interactors including ASC and Caspase-1 by co-

IP and determined T cells responses; respectively. We also determined both

extracellular and intracellular IL1β production by ELISA and western blotting,

as a maker for canonical inflammasome pathway activation. High expression

of NLRP11 and expression of costimulatory molecules made Daudi cells an

ideal model to use in our experiments. Given that B cells are professional

antigen presenting cells (APC) that interact with T cells, we co-cultured human

CD4+ primary T cells with Daudi cells in vitro. 40% down regulation of NLRP11

by siRNA in co-cultures resulted in the significant reduction of Th1, Th17

responses and an increase in anti-inflammatory response whereas did not

significantly affect Th2 responses when compared with control co-cultures.

In brief, our studies of NLRP11 suggest a role in regulating adaptive immune

responses.

Biography

Ceren Ciraci has completed her PhD from Iowa State University

and Postdoctoral Studies from University of Iowa Inflammation

Program. She is currently serving as a Junior Faculty at Istanbul

Technical University.

ciracic@itu.edu.tr

Downregulation of NLRP11 alters human T cell responses in co-

cultures with Daudi cells

Ceren Ciraci, İrem Ozel and ilgin Akkaya

Istanbul Technical University, Turkey