Fascinating Molecular and Immune Escape Mechanisms in the Treatment of STIs (Syphilis, Gonorrhea, Chlamydia, and Herpes Simplex).
Lucian G ScurtuViorel JingaOlga SimionescuPublished in: International journal of molecular sciences (2022)
The incidence of syphilis, gonorrhea, chlamydia, and herpes simplex has increased over the last decade, despite the numerous prevention strategies. Worldwide scientists report a surge in drug-resistant infections, particularly in immunocompromised patients. Antigenic variations in syphilis enable long-term infection, but benzathine penicillin G maintains its efficiency, whereas macrolides should be recommended with caution. Mupirocin and zoliflodacin were recently introduced as therapies against ceftriaxone-resistant gonococcus, which poses a larger global threat. The gastrointestinal and prostatic potential reservoirs of Chlamydia trachomatis may represent the key towards complete eradication. Similar to syphilis, macrolides resistance has to be considered in genital chlamydiosis. Acyclovir-resistant HSV may respond to the novel helicase-primase inhibitors and topical imiquimod, particularly in HIV-positive patients. Novel drugs can overcome these challenges while nanocarriers enhance their potency, particularly in mucosal areas. This review summarizes the most recent and valuable discoveries regarding the immunopathogenic mechanisms of these sexually transmitted infections and discusses the challenges and opportunities of the novel molecules and nanomaterials.
Keyphrases
- men who have sex with men
- hiv positive
- drug resistant
- human immunodeficiency virus
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- multidrug resistant
- prognostic factors
- drug delivery
- south africa
- patient reported outcomes
- antiretroviral therapy
- risk factors
- risk assessment
- pseudomonas aeruginosa
- helicobacter pylori
- climate change
- hiv infected
- acute respiratory distress syndrome
- human health
- ulcerative colitis
- benign prostatic hyperplasia
- extracorporeal membrane oxygenation