Adjuvanticity of a synthetic cord factor analogue for subunit Mycobacterium tuberculosis vaccination requires FcRγ–Syk–Card9–dependent innate immune activation

Author:

Werninghaus Kerstin12,Babiak Anna1,Groß Olaf3,Hölscher Christoph4,Dietrich Harald1,Agger Else Marie5,Mages Jörg1,Mocsai Attila6,Schoenen Hanne2,Finger Katrin3,Nimmerjahn Falk2,Brown Gordon D.7,Kirschning Carsten1,Heit Antje1,Andersen Peter5,Wagner Hermann1,Ruland Jürgen3,Lang Roland12

Affiliation:

1. Institute of Medical Microbiology, Immunology and Hygiene, Technical University Munich, D-81675 Munich, Germany

2. Molecular Medicine, Institute of Clinical Microbiology, University Hospital Erlangen, 91054 Erlangen, Germany

3. Department of Hematology, Technical University Munich, 80333 Munich, Germany

4. Division of Infection Immunology, Research Center Borstel, D-23845 Borstel, Germany

5. Adjuvant Research, Department of Infectious Disease Immunology, Statens Serum Institute, 2300 Copenhagen, Denmark

6. Semmelweis University School of Medicine, Budapest H-1089, Hungary

7. Division of Immunology, CLS, Institute for Infectious Diseases and Molecular Medicine, University of Cape Town, 7925 Cape Town, South Africa

Abstract

Novel vaccination strategies against Mycobacterium tuberculosis (MTB) are urgently needed. The use of recombinant MTB antigens as subunit vaccines is a promising approach, but requires adjuvants that activate antigen-presenting cells (APCs) for elicitation of protective immunity. The mycobacterial cord factor Trehalose-6,6-dimycolate (TDM) and its synthetic analogue Trehalose-6,6-dibehenate (TDB) are effective adjuvants in combination with MTB subunit vaccine candidates in mice. However, it is unknown which signaling pathways they engage in APCs and how these pathways are coupled to the adaptive immune response. Here, we demonstrate that these glycolipids activate macrophages and dendritic cells (DCs) via Syk–Card9–Bcl10–Malt1 signaling to induce a specific innate activation program distinct from the response to Toll-like receptor (TLR) ligands. APC activation by TDB and TDM was independent of the C-type lectin receptor Dectin-1, but required the immunoreceptor tyrosine-based activation motif–bearing adaptor protein Fc receptor γ chain (FcRγ). In vivo, TDB and TDM adjuvant activity induced robust combined T helper (Th)-1 and Th-17 T cell responses to a MTB subunit vaccine and partial protection against MTB challenge in a Card9-dependent manner. These data provide a molecular basis for the immunostimulatory activity of TDB and TDM and identify the Syk–Card9 pathway as a rational target for vaccine development against tuberculosis.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3