Underwhelming or Misunderstood? Genetic Variability of Pattern Recognition Receptors in Immune Responses and Resistance to Mycobacterium tuberculosis

• Published in: Frontiers in immunology 2021-06, Vol.12, p.714808-714808
• Main Authors: Dubé, Jean-Yves, Fava, Vinicius M, Schurr, Erwin, Behr, Marcel A
• Format: Article
• Language: English
• Subjects: Animals; Biomarkers; C-type lectin receptors (CLRs); Disease Resistance - genetics; Disease Resistance - immunology; genetic association studies (GAS); Genetic Predisposition to Disease; Genetic Variation; Host-Pathogen Interactions - genetics; Host-Pathogen Interactions - immunology; Humans; Immunity - genetics; Immunology; Lectins, C-Type - genetics; Lectins, C-Type - metabolism; Mice; Mice, Knockout; mycobacterium tuberculosis; Mycobacterium tuberculosis - immunology; NOD-like receptors (NLRs); pattern recognition receptor (PRR); Receptors, Pattern Recognition - genetics; tuberculosis; Tuberculosis - etiology
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2021.714808

Human genetic control is thought to affect a considerable part of the outcome of infection with ( ). Most of us deal with the pathogen by containment (associated with clinical "latency") or sterilization, but tragically millions each year do not. After decades of studies on host genetic susceptibility to infection, genetic variation has been discovered to play a role in tuberculous immunoreactivity and tuberculosis (TB) disease. Genes encoding pattern recognition receptors (PRRs) enable a consistent, molecularly direct interaction between humans and which suggests the potential for co-evolution. In this review, we explore the roles ascribed to PRRs during infection and ask whether such a longstanding and intimate interface between our immune system and this pathogen plays a critical role in determining the outcome of infection. The scientific evidence to date suggests that PRR variation is clearly implicated in altered immunity to but has a more subtle role in limiting the pathogen and pathogenesis. In contrast to 'effectors' like IFN-γ, IL-12, Nitric Oxide and TNF that are critical for control, 'sensors' like PRRs are less critical for the outcome of infection. This is potentially due to redundancy of the numerous PRRs in the innate arsenal, such that rarely goes unnoticed. Genetic association studies investigating PRRs during infection should therefore be designed to investigate endophenotypes of infection - such as immunological or clinical variation - rather than just TB disease, if we hope to understand the molecular interface between innate immunity and .