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      Marmosets as models of infectious diseases

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          Abstract

          Animal models of infectious disease often serve a crucial purpose in obtaining licensure of therapeutics and medical countermeasures, particularly in situations where human trials are not feasible, i.e., for those diseases that occur infrequently in the human population. The common marmoset ( Callithrix jacchus), a Neotropical new-world (platyrrhines) non-human primate, has gained increasing attention as an animal model for a number of diseases given its small size, availability and evolutionary proximity to humans. This review aims to (i) discuss the pros and cons of the common marmoset as an animal model by providing a brief snapshot of how marmosets are currently utilized in biomedical research, (ii) summarize and evaluate relevant aspects of the marmoset immune system to the study of infectious diseases, (iii) provide a historical backdrop, outlining the significance of infectious diseases and the importance of developing reliable animal models to test novel therapeutics, and (iv) provide a summary of infectious diseases for which a marmoset model exists, followed by an in-depth discussion of the marmoset models of two studied bacterial infectious diseases (tularemia and melioidosis) and one viral infectious disease (viral hepatitis C).

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          Regulatory T cells and immune tolerance.

          Regulatory T cells (Tregs) play an indispensable role in maintaining immunological unresponsiveness to self-antigens and in suppressing excessive immune responses deleterious to the host. Tregs are produced in the thymus as a functionally mature subpopulation of T cells and can also be induced from naive T cells in the periphery. Recent research reveals the cellular and molecular basis of Treg development and function and implicates dysregulation of Tregs in immunological disease.
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            Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC

            Human coronavirus-EMC (hCoV-EMC) is a new coronavirus that has killed around half of the few humans infected so far; this study now identifies DPP4 as the receptor that this virus uses to infect cells. Supplementary information The online version of this article (doi:10.1038/nature12005) contains supplementary material, which is available to authorized users.
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              Of Mice and Not Men: Differences between Mouse and Human Immunology

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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2527002Role: Role: Role:
                URI : https://loop.frontiersin.org/people/196351Role: Role:
                URI : https://loop.frontiersin.org/people/38290Role:
                Journal
                Front Cell Infect Microbiol
                Front Cell Infect Microbiol
                Front. Cell. Infect. Microbiol.
                Frontiers in Cellular and Infection Microbiology
                Frontiers Media S.A.
                2235-2988
                23 February 2024
                2024
                : 14
                : 1340017
                Affiliations
                [1] CBR Division, Defence Science and Technology Laboratory (Dstl) , Salisbury, United Kingdom
                Author notes

                Edited by: Namita Rout, Tulane University, United States

                Reviewed by: Deepa Machiah Kodandera, Emory Primate Research Center, United States

                Corinna Ross, Texas Biomedical Research Institute, United States

                *Correspondence: Ian C. T. Herron, iherron@ 123456dstl.gov.uk
                Article
                10.3389/fcimb.2024.1340017
                10921895
                38465237
                25bdb405-a087-42a1-b69e-fc575235df69
                Crown copyright © 2024 Dstl. Authors: Herron, Laws and Nelson

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 17 November 2023
                : 29 January 2024
                Page count
                Figures: 0, Tables: 6, Equations: 0, References: 424, Pages: 25, Words: 12435
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was funded by the UK Ministry of Defence Chief Scientific Advisor.
                Categories
                Cellular and Infection Microbiology
                Review
                Custom metadata
                Adaptive immunity in infection

                Infectious disease & Microbiology
                common marmoset,immunology,inflammation,animal models,francisella tularensis,burkholderia pseudomallei,hepatitis c virus

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