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  1. Article ; Online: C5aR

    Kim, Sae-Hae / Shim, Eun-Hyeon / Kim, Doo-Jin / Jang, Yong-Suk

    NPJ vaccines

    2023  Volume 8, Issue 1, Page(s) 120

    Abstract: The mucosal delivery route is considered ideal for immunization. However, induction of antigen-specific mucosal immunity is difficult due to the tolerogenic environment. Therefore, developing an immunogenic mucosal dendritic cell (DC)-targeting strategy ... ...

    Abstract The mucosal delivery route is considered ideal for immunization. However, induction of antigen-specific mucosal immunity is difficult due to the tolerogenic environment. Therefore, developing an immunogenic mucosal dendritic cell (DC)-targeting strategy is required. Herein, we investigated the characteristics and immunogenic potential of Peyer's patch (PP) DCs as an oral vaccination-targeting strategy. Single-cell RNA sequencing analysis of the PP DCs showed that complement C5a receptor- and lysozyme-expressing DCs exhibit increased expression of genes related to chemotaxis. Administration of the Co1 peptide, a C5aR ligand, increased CD8
    Language English
    Publishing date 2023-08-14
    Publishing country England
    Document type Journal Article
    ISSN 2059-0105
    ISSN (online) 2059-0105
    DOI 10.1038/s41541-023-00720-z
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Recent Insights into Cellular Crosstalk in Respiratory and Gastrointestinal Mucosal Immune Systems.

    Kim, Sae-Hae / Jang, Yong-Suk

    Immune network

    2020  Volume 20, Issue 6, Page(s) e44

    Abstract: The human body is continuously threatened by pathogens, and the immune system must maintain a balance between fighting infection and becoming over-activated. Mucosal surfaces cover several anatomically diverse organs throughout the body, such as the ... ...

    Abstract The human body is continuously threatened by pathogens, and the immune system must maintain a balance between fighting infection and becoming over-activated. Mucosal surfaces cover several anatomically diverse organs throughout the body, such as the respiratory and gastrointestinal tracts, and are directly exposed to the external environment. Various pathogens invade the body through mucosal surfaces, making the mucosa the frontline of immune defense. The immune systems of various mucosal tissues display distinctive features that reflect the tissues' anatomical and functional characteristics. This review discusses the cellular components that constitute the respiratory and gastrointestinal tracts; in particular, it highlights the complex interactions between epithelial and immune cells to induce Ag-specific immune responses in the lung and gut. This information on mucosal immunity may facilitate understanding of the defense mechanisms against infectious agents that invade mucosal surfaces, such as severe acute respiratory syndrome coronavirus 2, and provide insight into effective vaccine development.
    Language English
    Publishing date 2020-11-13
    Publishing country Korea (South)
    Document type Journal Article ; Review
    ZDB-ID 2536191-0
    ISSN 2092-6685 ; 1598-2629
    ISSN (online) 2092-6685
    ISSN 1598-2629
    DOI 10.4110/in.2020.20.e44
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Complement C5a promotes antigen cross-presentation by Peyer's patch monocyte-derived dendritic cells and drives a protective CD8

    Kim, Sae-Hae / Cho, Byeol-Hee / Kim, Kwang Soon / Jang, Yong-Suk

    Cell reports

    2021  Volume 35, Issue 2, Page(s) 108995

    Abstract: The complement fragment C5a is closely associated with adaptive immune induction in the mucosa. However, the mechanisms that control ... ...

    Abstract The complement fragment C5a is closely associated with adaptive immune induction in the mucosa. However, the mechanisms that control CD8
    MeSH term(s) Adaptive Immunity ; Animals ; Antigen Presentation ; Complement C5a/genetics ; Complement C5a/immunology ; Complement C5a/pharmacology ; Cross-Priming ; Dendritic Cells/drug effects ; Dendritic Cells/immunology ; Dendritic Cells/microbiology ; Female ; Gene Expression Profiling ; Gene Expression Regulation ; Immunity, Mucosal ; Intestinal Mucosa/drug effects ; Intestinal Mucosa/immunology ; Intestinal Mucosa/microbiology ; Listeria monocytogenes/immunology ; Listeria monocytogenes/pathogenicity ; Macrophages/drug effects ; Macrophages/immunology ; Macrophages/microbiology ; Mice ; Mice, Inbred BALB C ; Mice, Inbred C57BL ; Monocytes/drug effects ; Monocytes/immunology ; Monocytes/microbiology ; Muramidase/genetics ; Muramidase/immunology ; Peyer's Patches/drug effects ; Peyer's Patches/immunology ; Peyer's Patches/microbiology ; Reactive Oxygen Species/immunology ; Reactive Oxygen Species/metabolism ; Receptor, Anaphylatoxin C5a/genetics ; Receptor, Anaphylatoxin C5a/immunology ; Single-Cell Analysis ; T-Lymphocytes, Cytotoxic/drug effects ; T-Lymphocytes, Cytotoxic/immunology ; T-Lymphocytes, Cytotoxic/microbiology
    Chemical Substances Reactive Oxygen Species ; Receptor, Anaphylatoxin C5a ; Complement C5a (80295-54-1) ; Muramidase (EC 3.2.1.17)
    Language English
    Publishing date 2021-04-13
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2021.108995
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Yersinia enterocolitica

    Kim, Sae-Hae / Jang, Yong-Suk

    Immune network

    2017  Volume 17, Issue 4, Page(s) 228–236

    Abstract: In the intestinal mucosal surface, microfold cells (M cells) are the representative gateway for the uptake of luminal antigens. At the same time, M cells are the primary infection site for pathogens invading mucosal surface for their infection. Although ... ...

    Abstract In the intestinal mucosal surface, microfold cells (M cells) are the representative gateway for the uptake of luminal antigens. At the same time, M cells are the primary infection site for pathogens invading mucosal surface for their infection. Although it is well recognized that many mucosal pathogens exploit the M cells for their infection, the mechanism to infect M cells utilized by pathogens is not clearly understood yet. In this study, we found that M cells expressing complement 5a (C5a) receptor (C5aR) also express Toll-like receptor (TLR) 1/2 and TLR4. Infection of
    Language English
    Publishing date 2017-08-10
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2536191-0
    ISSN 2092-6685 ; 1598-2629
    ISSN (online) 2092-6685
    ISSN 1598-2629
    DOI 10.4110/in.2017.17.4.228
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: The development of mucosal vaccines for both mucosal and systemic immune induction and the roles played by adjuvants.

    Kim, Sae-Hae / Jang, Yong-Suk

    Clinical and experimental vaccine research

    2017  Volume 6, Issue 1, Page(s) 15–21

    Abstract: Vaccination is the most successful immunological practice that improves the quality of human life and health. Vaccine materials include antigens of pathogens and adjuvants potentiating the effectiveness of vaccination. Vaccines are categorized using ... ...

    Abstract Vaccination is the most successful immunological practice that improves the quality of human life and health. Vaccine materials include antigens of pathogens and adjuvants potentiating the effectiveness of vaccination. Vaccines are categorized using various criteria, including the vaccination material used and the method of administration. Traditionally, vaccines have been injected via needles. However, given that most pathogens first infect mucosal surfaces, there is increasing interest in the establishment of protective mucosal immunity, achieved by vaccination via mucosal routes. This review summarizes recent developments in mucosal vaccines and their associated adjuvants.
    Language English
    Publishing date 2017-01-25
    Publishing country Korea (South)
    Document type Journal Article ; Review
    ZDB-ID 2684652-4
    ISSN 2287-366X ; 2287-3651
    ISSN (online) 2287-366X
    ISSN 2287-3651
    DOI 10.7774/cevr.2017.6.1.15
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Complement C5a promotes antigen cross-presentation by Peyer’s patch monocyte-derived dendritic cells and drives a protective CD8+ T cell response

    Sae-Hae Kim / Byeol-Hee Cho / Kwang Soon Kim / Yong-Suk Jang

    Cell Reports, Vol 35, Iss 2, Pp 108995- (2021)

    2021  

    Abstract: Summary: The complement fragment C5a is closely associated with adaptive immune induction in the mucosa. However, the mechanisms that control CD8+ T cell responses by C5a have not been extensively explored. This study reveals that C5/C5a in the Peyer’s ... ...

    Abstract Summary: The complement fragment C5a is closely associated with adaptive immune induction in the mucosa. However, the mechanisms that control CD8+ T cell responses by C5a have not been extensively explored. This study reveals that C5/C5a in the Peyer’s patch (PP) subepithelial dome increases upon oral Listeria infection. We hypothesize that C5aR+ PP cells play an important role in the induction of antigen-specific T cell immunity. Using single-cell RNA sequencing, we identify C5aR- and lysozyme-expressing dendritic cells (C5aR+ LysoDCs) in PP and examine their role in CD8+ T cell immune induction. Stimulation of C5aR+ LysoDCs by C5a increases reactive oxygen species levels, leading to efficient antigen cross-presentation, which elicits an antigen-specific CD8+ T cell response. In C5-deficient mice, oral co-administration of C5a and Listeria enhances Listeria-specific cytotoxic T cell levels. Collectively, these findings suggest a role of the complement system in intestinal T cell immunity.
    Keywords C5a receptor ; CD8+ T cell ; complement C5a ; cross-presentation ; dendritic cells ; Peyer’s patch ; Biology (General) ; QH301-705.5
    Subject code 570
    Language English
    Publishing date 2021-04-01T00:00:00Z
    Publisher Elsevier
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  7. Article: N-terminal Domain of the Spike Protein of Porcine Epidemic Diarrhea Virus as a New Candidate Molecule for a Mucosal Vaccine.

    Kim, Sae-Hae / Cho, Byeol-Hee / Lee, Kyung-Yeol / Jang, Yong-Suk

    Immune network

    2018  Volume 18, Issue 3, Page(s) e21

    Abstract: Porcine epidemic diarrhea virus (PEDV) is a contagious coronavirus infecting pigs that leads to significant economic losses in the swine industry. Given that PEDV infection occurs in gut epithelial cells mainly via the fecal-oral route, induction of PEDV- ...

    Abstract Porcine epidemic diarrhea virus (PEDV) is a contagious coronavirus infecting pigs that leads to significant economic losses in the swine industry. Given that PEDV infection occurs in gut epithelial cells mainly via the fecal-oral route, induction of PEDV-specific immune responses in the mucosal compartment is required for protective immunity against viral infection. However, an effective mucosal vaccine against the currently prevalent PEDV strain is not available. In this study, we demonstrated that the N-terminal domain (NTD) of the spike (S) protein of PEDV represents a new vaccine candidate molecule to be applied via the mucosal route. We first established an
    Keywords covid19
    Language English
    Publishing date 2018-06-15
    Publishing country Korea (South)
    Document type Journal Article
    ZDB-ID 2536191-0
    ISSN 2092-6685 ; 1598-2629
    ISSN (online) 2092-6685
    ISSN 1598-2629
    DOI 10.4110/in.2018.18.e21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: C5a receptor targeting of partial non-structural protein 3 of dengue virus promotes antigen-specific IFN-γ-producing T-cell responses in a mucosal dengue vaccine model.

    Kim, Sae-Hae / Kim, Yu Na / Kim, Ju / Jang, Yong-Suk

    Cellular immunology

    2018  Volume 325, Page(s) 41–47

    Abstract: Mucosal vaccination is an ideal strategy to induce protective immunity in both mucosal and parenteral areas. Successful induction of an antigen-specific immune response via mucosal administration essentially requires the effective delivery of antigen ... ...

    Abstract Mucosal vaccination is an ideal strategy to induce protective immunity in both mucosal and parenteral areas. Successful induction of an antigen-specific immune response via mucosal administration essentially requires the effective delivery of antigen into a mucosal immune inductive site, which depends on antigen delivery into M cells. We previously reported that M cells specifically express C5aR, and antigen targeting to C5aR by using specific ligands, including Co1 peptide, promotes the antigen-specific immune response in both mucosal and systemic immune compartments. In this study, we found that application of the Co1 peptide to dengue virus antigen containing CD8 T cell epitopes effectively induced an antigen-specific IFN-γ-producing CD8
    MeSH term(s) Animals ; Antigens ; Antigens, Viral/immunology ; CD8-Positive T-Lymphocytes/immunology ; Dengue Vaccines/metabolism ; Dengue Virus/metabolism ; Disease Models, Animal ; Immunity, Mucosal/immunology ; Mice ; Mice, Inbred BALB C ; Mucous Membrane/immunology ; Receptor, Anaphylatoxin C5a/metabolism ; Vaccination ; Viral Nonstructural Proteins/immunology ; Viral Nonstructural Proteins/metabolism
    Chemical Substances Antigens ; Antigens, Viral ; Dengue Vaccines ; Receptor, Anaphylatoxin C5a ; Viral Nonstructural Proteins
    Language English
    Publishing date 2018-02-15
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80094-6
    ISSN 1090-2163 ; 0008-8749
    ISSN (online) 1090-2163
    ISSN 0008-8749
    DOI 10.1016/j.cellimm.2018.01.016
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Antigen targeting to M cells for enhancing the efficacy of mucosal vaccines.

    Kim, Sae-Hae / Jang, Yong-Suk

    Experimental & molecular medicine

    2014  Volume 46, Page(s) e85

    Abstract: Vaccination is one of the most successful applications of immunology and for a long time has depended on parenteral administration protocols. However, recent studies have pointed to the promise of mucosal vaccination because of its ease, economy and ... ...

    Abstract Vaccination is one of the most successful applications of immunology and for a long time has depended on parenteral administration protocols. However, recent studies have pointed to the promise of mucosal vaccination because of its ease, economy and efficiency in inducing an immune response not only systemically, but also in the mucosal compartment where many pathogenic infections are initiated. However, successful mucosal vaccination requires the help of an adjuvant for the efficient delivery of vaccine material into the mucosa and the breaking of the tolerogenic environment, especially in oral mucosal immunization. Given that M cells are the main gateway to take up luminal antigens and initiate antigen-specific immune responses, understanding the role and characteristics of M cells is crucial for the development of successful mucosal vaccines. Especially, particular interest has been focused on the regulation of the tolerogenic mucosal microenvironment and the introduction of the luminal antigen into the lymphoid organ by exploiting the molecules of M cells. Here, we review the characteristics of M cells and the immune regulatory factors in mucosa that can be exploited for mucosal vaccine delivery and mucosal immune regulation.
    MeSH term(s) Administration, Oral ; Animals ; Antigens, Bacterial/immunology ; Antigens, Viral/immunology ; Bacterial Vaccines/administration & dosage ; Bacterial Vaccines/immunology ; Humans ; Immunity, Mucosal ; Intestinal Mucosa/cytology ; Intestinal Mucosa/immunology ; Peyer's Patches/cytology ; Peyer's Patches/immunology ; Viral Vaccines/administration & dosage ; Viral Vaccines/immunology
    Chemical Substances Antigens, Bacterial ; Antigens, Viral ; Bacterial Vaccines ; Viral Vaccines
    Language English
    Publishing date 2014-03-14
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Review
    ZDB-ID 1328915-9
    ISSN 2092-6413 ; 1226-3613 ; 0378-8512
    ISSN (online) 2092-6413
    ISSN 1226-3613 ; 0378-8512
    DOI 10.1038/emm.2013.165
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Cutting Edge: LL-37-Mediated Formyl Peptide Receptor-2 Signaling in Follicular Dendritic Cells Contributes to B Cell Activation in Peyer's Patch Germinal Centers.

    Kim, Sae-Hae / Kim, Yu Na / Jang, Yong-Suk

    Journal of immunology (Baltimore, Md. : 1950)

    2016  Volume 198, Issue 2, Page(s) 629–633

    Abstract: Peyer's patches (PPs) are the major mucosal immune-inductive site, and germinal centers (GCs) in PPs determine the quality of the Abs produced. PP GCs are continuously induced by the gut microbiota, and their maintenance contributes to the induction of ... ...

    Abstract Peyer's patches (PPs) are the major mucosal immune-inductive site, and germinal centers (GCs) in PPs determine the quality of the Abs produced. PP GCs are continuously induced by the gut microbiota, and their maintenance contributes to the induction of strong IgA responses to Ags. In this study, we investigated the role of formyl peptide receptor (FPR)-mediated signaling in the maintenance of PP GCs, because FPRs recognize the microbiota and initiate an innate immune response by chemotaxis. We found that follicular dendritic cells (FDCs), a key organizer of B cell follicles and GCs in mucosal immunity, express Fpr2. Additionally, Fpr2-mediated signaling in PP FDCs promoted Cxcl13 and B cell activating factor expression, as well as B cell proliferation and activation. Therefore, we suggest that Fpr2-mediated signaling in FDCs plays a key role in GC maintenance in PPs and results in an Ag-specific IgA response in the gut mucosal immune compartment.
    MeSH term(s) Animals ; Antimicrobial Cationic Peptides/immunology ; B-Lymphocytes/immunology ; Dendritic Cells, Follicular/immunology ; Flow Cytometry ; Fluorescent Antibody Technique ; Germinal Center/immunology ; Immunity, Mucosal/immunology ; Lymphocyte Activation/immunology ; Mice ; Mice, Inbred BALB C ; Peyer's Patches/immunology ; Real-Time Polymerase Chain Reaction ; Receptors, Formyl Peptide/immunology ; Signal Transduction/immunology
    Chemical Substances Antimicrobial Cationic Peptides ; Receptors, Formyl Peptide ; formyl peptide receptor 2, mouse ; ropocamptide (3DD771JO2H)
    Language English
    Publishing date 2016-12-14
    Publishing country United States
    Document type Journal Article
    ZDB-ID 3056-9
    ISSN 1550-6606 ; 0022-1767 ; 1048-3233 ; 1047-7381
    ISSN (online) 1550-6606
    ISSN 0022-1767 ; 1048-3233 ; 1047-7381
    DOI 10.4049/jimmunol.1600886
    Database MEDical Literature Analysis and Retrieval System OnLINE

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