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Innate and Adaptive Immune Response to Bacterial, Viral and Fungal Infections

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Microbiology".

Deadline for manuscript submissions: closed (30 September 2023) | Viewed by 4569

Special Issue Editor


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Guest Editor
Center for Gender Specific Medicine, Istituto Superiore di Sanità, 00161 Rome, Italy
Interests: anti-infective immune response; lipid rafts and infections; sex differences in the immune response

Special Issue Information

Dear Colleagues,

The immune system refers to a variety of cells and processes that have the crucial role of protecting the skin, respiratory, and intestinal tracts and other areas of our body from foreign antigens such as bacteria, fungi and viruses. The first line of defense is represented by the non-antigen-specific innate immune arm, which is exploited by the host immediately after encountering the microbial pathogen. Besides anatomical and physiological barriers, several innate immune cells are involved in this first defense, such as macrophages, dendritic cells, neutrophils, basophils, eosinophils, mast cells, natural killer cells and innate lymphoid cells. These cells exploit a vast array of pathogen-recognition receptors (PRRs) to detect common structures of several microbes known as pathogen-associated molecular patterns (PAMPs), such as bacterial lipopolysaccharides or double-stranded ribonucleic acid produced during viral infections. Microbial phagocytosis and killing by phagocytic cells as well as prompt cytokine and chemokine production at the site of infection are responsible for the first defense, inflammation and recruitment of immune cells. The complement system takes part in the innate immune response by targeting and opsonizing several microbial pathogens, thereby facilitating phagocytosis and killing.

The second line of defense is represented by the adaptive immune response, which specifically recognizes microbial antigens, eliminates infected cells and develops a long-term immunological memory. T lymphocytes after antigen presentation by professional antigen-presenting cells proliferate and exert their effector functions, and B lymphocytes differentiate into plasma cells to produce antibodies.

Females have both innate and acquired immunological responses stronger than males due to biological factors (i.e., genetic and epigenetic factors or sex hormones) and to psychosocial factors (i.e., gender differences). In particular, females show a more effective phagocytosis and antigen presentation, a stronger production of cytokines in response to infections, a higher absolute number of CD4 + T lymphocytes and higher levels of circulating antibodies in comparison to males. The increased activation of the immune response is a double-edged sword because it makes females more resistant to some infections but more susceptible to inflammatory and autoimmune diseases. Males and females of certain species, ranging from humans to horses and rodents, differ in their responses to and the outcomes of diverse pathogenic infections. In most cases, the precise mechanism mediating the dimorphism in infectious disease pathogenesis is not known, in part because sex has not been evaluated as a biological variable for the analysis of outcome data.

This Special Issue will explore new insights in the study of cellular mechanisms involved both in the innate and acquired immune response to bacteria, fungi, viruses and parasites, also taking into account sex differences in infectious disease pathogenesis.

Dr. Maria Cristina Gagliardi 
Guest Editor

Manuscript Submission Information

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Keywords

  • innate immune cells
  • inflammatory/antinflammatory cytokines
  • antigen presenting cells
  • complement
  • antimicrobial T and B cell response
  • sexual dymorphism

Published Papers (3 papers)

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Research

13 pages, 2039 KiB  
Article
Pseudomonas aeruginosa-Derived DnaJ Induces the Expression of IL−1β by Engaging the Interplay of p38 and ERK Signaling Pathways in Macrophages
by Dae-Kyum Kim, Jin-Won Huh, Hyeonseung Yu, Yeji Lee, Yongxin Jin and Un-Hwan Ha
Int. J. Mol. Sci. 2023, 24(21), 15957; https://doi.org/10.3390/ijms242115957 - 03 Nov 2023
Cited by 1 | Viewed by 720
Abstract
As members of pathogen-associated molecular patterns, bacterial heat shock proteins (HSPs) are widely recognized for their role in initiating innate immune responses. This study aimed to examine the impact of DnaJ, a homolog of HSP40 derived from Pseudomonas aeruginosa (P. aeruginosa), [...] Read more.
As members of pathogen-associated molecular patterns, bacterial heat shock proteins (HSPs) are widely recognized for their role in initiating innate immune responses. This study aimed to examine the impact of DnaJ, a homolog of HSP40 derived from Pseudomonas aeruginosa (P. aeruginosa), on the regulation of IL−1β expression in macrophages. We demonstrated that DnaJ modulates macrophages to secrete IL−1β by activating NF-κB and MAPK signaling pathways. Specifically, ERK was identified as a positive mediator for IL−1β expression, while p38 acted as a negative mediator. These results suggest that the reciprocal actions of these two crucial MAPKs play a vital role in controlling IL−1β expression. Additionally, the reciprocal actions of MAPKs were found to regulate the activation of inflammasome-related molecules, including vimentin, NLRP3, caspase-1, and GSDMD. Furthermore, our investigation explored the involvement of CD91/CD40 in ERK signaling-mediated IL−1β production from DnaJ-treated macrophages. These findings emphasize the importance of understanding the signaling mechanisms underlying IL−1β induction and suggest the potential utility of DnaJ as an adjuvant for stimulating inflammasome activation. Full article
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20 pages, 2090 KiB  
Article
Molecular Signatures in Swine Innate and Adaptive Immune Responses to African Swine Fever Virus Antigens p30/p54/CD2v Expressed Using a Highly Efficient Semliki Forest Virus Replicon System
by Mei Huang, Hanghui Zheng, Weixiong Tan, Chengwei Xiang, Niran Fang, Wenting Xie, Lianghai Wen, Dingxiang Liu and Ruiai Chen
Int. J. Mol. Sci. 2023, 24(11), 9316; https://doi.org/10.3390/ijms24119316 - 26 May 2023
Cited by 1 | Viewed by 1983
Abstract
African swine fever virus (ASFV) causes a devastating viral hemorrhagic disease in domestic pigs and Eurasian wild boars, posing a foremost threat to the swine industry and pig farming. The development of an effective vaccine is urgently needed, but has been hampered by [...] Read more.
African swine fever virus (ASFV) causes a devastating viral hemorrhagic disease in domestic pigs and Eurasian wild boars, posing a foremost threat to the swine industry and pig farming. The development of an effective vaccine is urgently needed, but has been hampered by the lack of an in-depth, mechanistic understanding of the host immune response to ASFV infection and the induction of protective immunity. In this study, we report that immunization of pigs with Semliki Forest Virus (SFV) replicon-based vaccine candidates expressing ASFV p30, p54, and CD2v, as well as their ubiquitin-fused derivatives, elicits T cell differentiation and expansion, promoting specific T cell and humoral immunity. Due to significant variations in the individual non-inbred pigs in response to the vaccination, a personalized analysis was conducted. Using integrated analysis of differentially expressed genes (DEGs), Venn, KEGG and WGCNA, Toll-like receptor, C-type lectin receptor, IL17 receptor, NOD-like receptor and nucleic acid sensor-mediated signaling pathways were demonstrated to be positively correlated to the antigen-stimulated antibody production and inversely correlated to the IFN-γ secreting cell counts in peripheral blood mononuclear cells (PBMCs). An up-regulation of CIQA, CIQB, CIQC, C4BPA, SOSC3, S100A8 and S100A9, and down-regulation of CTLA4, CXCL2, CXCL8, FOS, RGS1, EGR1 and SNAI1 are general in the innate immune response post-the second boost. This study reveals that pattern recognition receptors TLR4, DHX58/DDX58 and ZBP1, and chemokines CXCL2, CXCL8 and CXCL10 may play important roles in regulating this vaccination-stimulated adaptive immune response. Full article
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18 pages, 4089 KiB  
Article
Immunogenic Properties and Antigenic Similarity of Virus-like Particles Derived from Human Polyomaviruses
by Asta Lučiūnaitė, Indrė Dalgėdienė, Emilija Vasiliūnaitė, Milda Norkienė, Indrė Kučinskaitė-Kodzė, Aurelija Žvirblienė and Alma Gedvilaitė
Int. J. Mol. Sci. 2023, 24(5), 4907; https://doi.org/10.3390/ijms24054907 - 03 Mar 2023
Viewed by 1418
Abstract
Polyomaviruses (PyVs) are highly prevalent in humans and animals. PyVs cause mild illness, however, they can also elicit severe diseases. Some PyVs are potentially zoonotic, such as simian virus 40 (SV40). However, data are still lacking about their biology, infectivity, and host interaction [...] Read more.
Polyomaviruses (PyVs) are highly prevalent in humans and animals. PyVs cause mild illness, however, they can also elicit severe diseases. Some PyVs are potentially zoonotic, such as simian virus 40 (SV40). However, data are still lacking about their biology, infectivity, and host interaction with different PyVs. We investigated the immunogenic properties of virus-like particles (VLPs) derived from viral protein 1 (VP1) of human PyVs. We immunised mice with recombinant HPyV VP1 VLPs mimicking the structure of viruses and compared their immunogenicity and cross-reactivity of antisera using a broad spectrum of VP1 VLPs derived from the PyVs of humans and animals. We demonstrated a strong immunogenicity of studied VLPs and a high degree of antigenic similarity between VP1 VLPs of different PyVs. PyV-specific monoclonal antibodies were generated and applied for investigation of VLPs phagocytosis. This study demonstrated that HPyV VLPs are highly immunogenic and interact with phagocytes. Data on the cross-reactivity of VP1 VLP-specific antisera revealed antigenic similarities among VP1 VLPs of particular human and animal PyVs and suggested possible cross-immunity. As the VP1 capsid protein is the major viral antigen involved in virus-host interaction, an approach based on the use of recombinant VLPs is relevant for studying PyV biology regarding PyV interaction with the host immune system. Full article
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