hh.sePublications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Polymer Chemistry Defines Adjuvant Properties and Determines the Immune Response against the Antigen or Vaccine
Texas Tech University, Lubbock, United States.ORCID iD: 0000-0002-8907-7009
Halmstad University, School of Business, Innovation and Sustainability.ORCID iD: 0000-0001-7790-8197
2023 (English)In: Vaccines, E-ISSN 2076-393X, Vol. 11, no 9, article id 1395Article, review/survey (Refereed) Published
Abstract [en]

Activation of the immune system is a needed for designing new antigen/drug delivery systems to develop new therapeutics and for developing animal disease models to study the disease pathogenesis. A weak antigen alone is insufficient to activate the immune system. Sometimes, assistance in the form of polymers is needed to control the release of antigens under in vivo conditions or in the form of an adjuvant to activate the immune system efficiently. Many kinds of polymers from different functional groups are suitable as microbial antigens for inducing therapeutic immune responses against infectious diseases at the preclinical level. The choice of the functionality of polymer varies as per the application type. Polymers from the acid and ester groups are the most common types investigated for protein-based antigens. However, electrostatic interaction-displaying polymers like cationic polymers are the most common type for nucleic acid-based antigens. Metal coordination chemistry is commonly used in polymers designed for cancer immunotherapeutic applications to suppress inflammation and induce a protective immune response. Amide chemistry is widely deployed in polymers used to develop antigen-specific disease models like the experimental autoimmune arthritis murine model. © 2023 by the authors.

Place, publisher, year, edition, pages
Basel: MDPI, 2023. Vol. 11, no 9, article id 1395
Keywords [en]
antigen, autoimmunity, cancer, drug delivery, functional moiety, immune response, polymer, polymer chemistry
National Category
Immunology in the medical area
Identifiers
URN: urn:nbn:se:hh:diva-51779DOI: 10.3390/vaccines11091395ISI: 001077857300001PubMedID: 37766073Scopus ID: 2-s2.0-85172220185OAI: oai:DiVA.org:hh-51779DiVA, id: diva2:1812876
Available from: 2023-11-17 Created: 2023-11-17 Last updated: 2025-10-01Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMedScopus

Authority records

Nandakumar, Kutty Selva

Search in DiVA

By author/editor
Shakya, Akhilesh KumarNandakumar, Kutty Selva
By organisation
School of Business, Innovation and Sustainability
In the same journal
Vaccines
Immunology in the medical area

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 36 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf