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210512 ||| eng |
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|a 9782889454617
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|a 978-2-88945-461-7
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100 |
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|a Francesca Chiodi
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245 |
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|a HIV-Induced Damage of B Cells and Production of HIV Neutralizing Antibodies
|h Elektronische Ressource
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260 |
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|b Frontiers Media SA
|c 2018
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300 |
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|a 1 electronic resource (171 p.)
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653 |
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|a Gene Expression
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653 |
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|a BAFF
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653 |
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|a clinical potential of HIV-1 antibodies
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653 |
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|a auto-antibodies to CCR5
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653 |
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|a mucosal IgA responses
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653 |
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|a Medicine / bicssc
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653 |
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|a B cells
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653 |
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|a HIV-1 vaccine targets
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653 |
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|a neutralizing and non neutralizing HIV-1 antibodies
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653 |
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|a maternal HIV antibodies
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653 |
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|a CXCL13
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653 |
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|a FcRL4
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700 |
1 |
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|a Gabriella Scarlatti
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041 |
0 |
7 |
|a eng
|2 ISO 639-2
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|b DOAB
|a Directory of Open Access Books
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|a Frontiers Research Topics
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|a Creative Commons (cc), https://creativecommons.org/licenses/by/4.0/
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8 |
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|a 10.3389/978-2-88945-461-7
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856 |
4 |
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|u https://www.frontiersin.org/research-topics/5357/hiv-induced-damage-of-b-cells-and-production-of-hiv-neutralizing-antibodies
|7 0
|x Verlag
|3 Volltext
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856 |
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|u https://directory.doabooks.org/handle/20.500.12854/49485
|z DOAB: description of the publication
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|a 610
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|a Multiple dysfunctions take place in the B cell compartment during HIV-1 infection, comprising depletion of resting memory B cells carrying serological memory to vaccines and previously met pathogens. In addition, population of B cells characterized by the expression of exhaustion markers are enlarged during HIV-1 infection. Antibodies with the capacity to neutralize a broad range of HIV-1 isolates can be detected only in a minority of infected patients, after a year or more from acute infection. An open question is whether the inability of producing neutralizing HIV-1 antibodies is somehow linked to the B cell immunopathology observed in patients. In this research topic we invited scientists to summarize the current state of knowledge on regulation and development of B cells and antibody responses during HIV-1 infection; fifteen contributions were received comprising both reviews and original articles. The articles are related to B cell dysfunctions identified in HIV-1 infected individuals, production of different types of antibodies (neutralizing versus non neutralizing, and of different isotypes) in vivo during HIV-1 infection and the biological factors which may impact on this process, clinical potential and applications of anti-HIV antibodies and how to achieve neutralizing antibody responses to HIV-1 epitopes upon vaccination. The topic has gathered articles on front-line research undertaken in the field of B cells and antibodies in HIV-1 infection. It is our hope that the collection of articles presented in this book may be useful for new and experienced scholars in the field and add a piece to the complex puzzle of knowledge needed for the development of an HIV-1 vaccine.
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