Immune Cell Migration and Vaccination

A special issue of Vaccines (ISSN 2076-393X).

Deadline for manuscript submissions: closed (31 August 2021) | Viewed by 9673

Special Issue Editors


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Guest Editor
Department of Medicine, Division of Immunolgy, Friedrich-Alexander-Universität, 91054 Erlangen, Germany

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Co-Guest Editor
Charité – Universitätsmedizin Berlin, Berlin, Germany
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Special Issue Information

Dear Colleagues,

Vaccination has been proven to be one of the most powerful achievements for human health. Nevertheless, the current pandemic shows that new infectious threats for mankind can enter the stage anytime, with unforeseeable dynamics and impact. Therefore, we need to understand better how effective vaccines elicit protective and long-lasting immunity. In the case of systemic infectious diseases, different layers of the immune system are challenged in different tissues. The information about an invading pathogen needs to be disseminated throughout the body, for instance, by cells of the innate immune system, without causing harm. Adaptive immunity requires the transformation of this information through the refined spatial and temporal coordination of migrating immune cells. Henceforth, the establishment of immunity depends crucially on the ability of immune cells to migrate and to communicate systemically. The failure of appropriate migration can lead to immunodeviation or immunodeficiency. Besides inducing humoral immunity via the controlled exit of memory and plasma cells from germinal centers, efficient antiviral vaccines also need to elicit memory T cell responses. Recent progress has been made in identifying general mechanisms of B cell germinal center exit and the localization of memory T cells. Memory B cells, memory plasma cells, and memory T cells migrate to protective tissue niches, forming tissue-resident memory. Eventually, memory cells encounter an antigen for a second time, which leads to their engagement in secondary immune responses in different microanatomic structures in various organs. We propose that a multifaceted view of the role of immune cell migration and specific anatomical structures, as well as of new techniques, will aid in better understanding the establishment of protective immunity. This may assist us during the current and potential future challenges.

We invite you to contribute manuscripts containing original data or review articles expressing your opinion about the role of immune cell migration during vaccination and long-lasting immunity and how manipulation of cytoskeletal elements may deviate—or speed up—immune responses.

Prof. Dr. Dirk Mielenz
Prof. Dr. Anja Erika Hauser
Guest Editors

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. Vaccines is an international peer-reviewed open access monthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 2700 CHF (Swiss Francs). Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Vaccination
  • B lymphocyte
  • T lymphocyte
  • dendritic cell
  • inflammation
  • migration
  • lymph node
  • blood vessel
  • cytoskeleton
  • intravital imaging

Published Papers (2 papers)

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Review

17 pages, 1134 KiB  
Review
Krüppel-like Factor 2 (KLF2) in Immune Cell Migration
by Jens Wittner and Wolfgang Schuh
Vaccines 2021, 9(10), 1171; https://doi.org/10.3390/vaccines9101171 - 13 Oct 2021
Cited by 19 | Viewed by 5471
Abstract
Krüppel-like factor 2 (KLF2), a transcription factor of the krüppel-like family, is a key regulator of activation, differentiation, and migration processes in various cell types. In this review, we focus on the functional relevance of KLF2 in immune cell migration and homing. We [...] Read more.
Krüppel-like factor 2 (KLF2), a transcription factor of the krüppel-like family, is a key regulator of activation, differentiation, and migration processes in various cell types. In this review, we focus on the functional relevance of KLF2 in immune cell migration and homing. We summarize the key functions of KLF2 in the regulation of chemokine receptors and adhesion molecules and discuss the relevance of the KLF2-mediated control of immune cell migration in the context of immune responses, infections, and diseases. Full article
(This article belongs to the Special Issue Immune Cell Migration and Vaccination)
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20 pages, 1037 KiB  
Review
T Cell/B Cell Interactions in the Establishment of Protective Immunity
by Julia Ritzau-Jost and Andreas Hutloff
Vaccines 2021, 9(10), 1074; https://doi.org/10.3390/vaccines9101074 - 24 Sep 2021
Cited by 8 | Viewed by 3444
Abstract
Follicular helper T cells (Tfh) are the T cell subset providing help to B cells for the generation of high-affinity antibodies and are therefore of key interest for the development of vaccination strategies against infectious diseases. In this review, we will discuss how [...] Read more.
Follicular helper T cells (Tfh) are the T cell subset providing help to B cells for the generation of high-affinity antibodies and are therefore of key interest for the development of vaccination strategies against infectious diseases. In this review, we will discuss how the generation of Tfh cells and their interaction with B cells in secondary lymphoid organs can be optimized for therapeutic purposes. We will summarize different T cell subsets including Tfh-like peripheral helper T cells (Tph) capable of providing B cell help. In particular, we will highlight the novel concept of T cell/B cell interaction in non-lymphoid tissues as an important element for the generation of protective antibodies directly at the site of pathogen invasion. Full article
(This article belongs to the Special Issue Immune Cell Migration and Vaccination)
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