Immunological and Antimicrobial Adjuvants from Marine Sources

A special issue of Marine Drugs (ISSN 1660-3397).

Deadline for manuscript submissions: closed (5 February 2021) | Viewed by 5215

Special Issue Editor


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Guest Editor
Department of Biochemistry, Microbiology and Biotechnology, Far Eastern Federal University, Vladivostok, Russia
Interests: structure and function of biological membranes; lipids; phase transitons; marine hydrobionts; bacteria; adaptation; antibiotic resistance; lipid-dependent conformation and functions of proteins; lipochaperoning; vaccines; adjuvant vehicles; recombinant proteins; viruses; nanobiotechnology; immunology
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Special Issue Information

Dear Colleagues,

The protection of macroorganisms (humans and animals) from pathogenic microorganisms depends both on the state of the macroorganism's immune system and on the sensitivity of microorganisms to antibiotics. To increase the effectiveness of the corresponding mechanisms, immunological and antimicrobial adjuvants are used, respectively.

Immunological adjuvant is a substance or complex of substances, including adjuvant delivery systems, that is administered with an antigen to boost or modifies the immune response to that target antigen. Recently, there has been an active use of adjuvants in the immunotherapy of tumors, since cancer is associated with impaired functioning of the immune system.

An immunological adjuvant is a substance or complex of substances, including adjuvant delivery systems, which is administered with an antigen to boost (immunostimulation) and/or modulate (immunomodulation) the immune response to that target antigen. Immunological adjuvants differ in their effect on adaptive and innate immunity, which is actually associated with the involvement of T-cells responsible for recognizing antigen, B-lymphocytes, producing antibodies, and innate immunity cells. Recently, there has been an active use of adjuvants in the immunotherapy of tumors (Adjuvant immunotherapy for cancer), since cancer is associated with impaired functioning of the immune system. 

On the other hand, increasing the effectiveness of vaccines can help to solve another global problem associated with a permanent widening list of pathogens resistant to antimicrobials. This problem primarily relates to antibiotic resistance of bacteria. Therefore, the use of adjuvants for antibiotics and other antimicrobial chemotherapeutic drugs is a new and one of the most effective strategies for restoring the sensitivity (resensitization) of pathogens to conventional antimicrobials. Antimicrobial adjuvants can directly act on the microbe and block the pathogen resistance to antimicrobials or enhance their effect by acting on the protective mechanisms of the macroorganism.

Marine organisms are abundant in biologically active substances. Some of them possess an adjuvant activity. The main goal of this Special Issue on “Marine-Derived Immunological and Antimicrobial Adjuvants” is to summarize the achievements in the field of the search for substances of marine origin and their semi-synthetic derivatives that possess adjuvant activity. Research articles and reviews devoted to mechanisms of actions of such adjuvants are also welcome.

Dr. Nina M. Sanina
Guest Editor

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Published Papers (2 papers)

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Research

13 pages, 4573 KiB  
Article
Computational Assessment of Chito-Oligosaccharides Interactions with Plasma Proteins
by Diana Larisa Roman, Vasile Ostafe and Adriana Isvoran
Mar. Drugs 2021, 19(3), 120; https://doi.org/10.3390/md19030120 - 24 Feb 2021
Cited by 6 | Viewed by 2132
Abstract
It is widely rec ognized that chitin and chitosan are potential sources of bioactive materials and that their oligosaccharides reveal various biological activities (including antimicrobial) that are correlated with their structures and physicochemical properties. This study uses the molecular docking approach to assess [...] Read more.
It is widely rec ognized that chitin and chitosan are potential sources of bioactive materials and that their oligosaccharides reveal various biological activities (including antimicrobial) that are correlated with their structures and physicochemical properties. This study uses the molecular docking approach to assess the interactions of small chito-oligosaccharides (MW< 1500 Da) with plasma proteins in order to obtain information regarding their fate of distribution in the human organism. There are favorable interactions of small chito-oligomers with plasma proteins, the interactions with human serum albumin being stronger than those with α-1-acid glycoprotein. The interaction energies increase with increasing the molecular weight, decrease with increasing deacetylation degrees and are reliant on the deacetylation pattern. This study could inform the application of chito-oligosaccharides with varying molecular weights, degrees, and patterns of deacetylation in human health. Full article
(This article belongs to the Special Issue Immunological and Antimicrobial Adjuvants from Marine Sources)
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13 pages, 2636 KiB  
Article
Human Peripheral Blood Dendritic Cell and T Cell Activation by Codium fragile Polysaccharide
by Wei Zhang, Juyoung Hwang, Hae-Bin Park, Seong-Min Lim, Seulgi Go, Jihoe Kim, Inho Choi, Sangguan You and Jun-O Jin
Mar. Drugs 2020, 18(11), 535; https://doi.org/10.3390/md18110535 - 27 Oct 2020
Cited by 17 | Viewed by 2658
Abstract
Natural polysaccharides exhibit an immunostimulatory effect with low toxicity in humans and animals. It has shown that polysaccharide extracted from Codium fragile (CFP) induces anti-cancer immunity by dendritic cell (DC) activation, while the effect of CFP has not examined in the human immune [...] Read more.
Natural polysaccharides exhibit an immunostimulatory effect with low toxicity in humans and animals. It has shown that polysaccharide extracted from Codium fragile (CFP) induces anti-cancer immunity by dendritic cell (DC) activation, while the effect of CFP has not examined in the human immune cells. In this study, we found that CFP promoted the upregulation of CD80, CD83 and CD86 and major histocompatibility complex (MHC) class I and II in human monocyte-derived dendritic cells (MDDCs). In addition, CFP induced the production of proinflammatory cytokines in MDDCs. Moreover, CFP directly induced the activation of Blood Dendritic Cell Antigen (BDCA)1+ and BDCA3+ subsets of human peripheral blood DCs (PBDCs). The CFP-stimulated BDCA1+ PBDCs further promoted activation and proliferation of syngeneic CD4 T cells. The CFP-activated BDCA3+ PBDCs activated syngeneic CD8 T cells, which produced cytotoxic mediators, namely, cytotoxic T lymphocytes. These results suggest that CFP may be a candidate molecule for enhancing immune activation in humans. Full article
(This article belongs to the Special Issue Immunological and Antimicrobial Adjuvants from Marine Sources)
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