Nama : Sintia Widyo Wati
NPM : 2A214304
Kelas : 3EB24
NPM : 2A214304
Kelas : 3EB24
Conjugate Vaccine Immunotherapy for Substance Use
Disorder
Paul T. Bremer and Kim D. Janda
Eric L. Barker, ASSOCIATE EDITOR
Pharmacological Reviews July 2017, 69 (3) 298-315;
DOI: https://doi.org/10.1124/pr.117.013904
ArticleFigures & DataInfo & MetricseLetters
PDF
Abstract
Substance
use disorder, especially in relation to opioids such as heroin and fentanyl, is
a significant public health issue and has intensified in recent years. As a
result, substantial interest exists in developing therapeutics to counteract
the effects of abused drugs. A promising universal strategy for antagonizing
the pharmacology of virtually any drug involves the development of a conjugate
vaccine, wherein a hapten structurally similar to the target drug is conjugated
to an immunogenic carrier protein. When formulated with adjuvants and
immunized, the immunoconjugate should elicit serum IgG antibodies with the
ability to sequester the target drug to prevent its entry to the brain, thereby
acting as an immunoantagonist. Despite the failures of first-generation
conjugate vaccines against cocaine and nicotine in clinical trials,
second-generation vaccines have shown dramatically improved performance in
preclinical models, thus renewing the potential clinical utility of conjugate
vaccines in curbing substance use disorder. This review explores the critical
design elements of drug conjugate vaccines such as hapten structure, adjuvant
formulation, bioconjugate chemistry, and carrier protein selection. Methods for
evaluating these vaccines are discussed, and recent progress in vaccine
development for each drug is summarized.
Footnotes
This work was supported by National Institutes of
Health National Institute on Drug Abuse [Grants R01DA008590, R01DA026625,
R21DA039634, and UH2DA041146].
sumber : http://pharmrev.aspetjournals.org/content/69/3/298
Tidak ada komentar:
Posting Komentar