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Monoclonal Antibodies Against Infectious Microbes: So Long and Too Little!
Gerard M Raj1, Rekha Priyadarshini2, Sakthibalan Murugesan1
1Department of Pharmacology, Sri Venkateshwaraa Medical College Hospital and Research Centre (SVMCH & RC), Puducherry 605102, India.
Abstract:
Monoclonal antibodies (mAbs) as alternatives or more often as complementary to the conventional antimicrobials have been developed for the management of infectious conditions for the past two decades. These pharmacotherapeutic strategies are inevitable as the burden of antimicrobial resistance is far-reaching in recent times. MAbs are part of the targeted pharmacotherapy armamentarium with a high degree of specificity - hence, exert comparatively superior efficacy and tolerability than the conventional polyclonal antisera. So far, only five mAbs have been approved for the management of infectious states, since the marketing authorization (1998) given to palivizumab (Synagis®) for the prophylaxis of lower respiratory tract disease caused by a respiratory syncytial virus in pediatric patients. Ibalizumab-uiyk (Trogarzo™) used for the management of multidrug-resistant HIV-1 infection not yielding to at least 10 antiretroviral drugs, was approved recently. Among the three antibacterial mAbs, raxibacumab (ABthrax®/ Anthrin®) and obiltoxaximab (Anthim®) are indicated for the treatment and prophylaxis of inhalation anthrax due to Bacillus anthracis; bezlotoxumab (Zinplava®) is used to reduce the recurrence of Clostridium difficile infection. There are also around 30 and 15 mAbs in different phases of development for viral and bacterial conditions. As alternatives to the traditional antivirals and antibacterials, the antimicrobial mAbs are the need of the hour. These mAbs are more relevant to the management of conditions like emerging viral outbreaks wherein there is a lack of prophylactic vaccines. The current cutting-edge engineering technologies revolutionizing the production of mAbs include phagedisplayed antibody libraries, cloning from single-memory B cells or single-antibody-secreting plasma B cells, proteomics-directed cloning of mAbs from serum clubbed with high-throughput sequencing techniques. Yet, the cost of manufacture continues to be the main limiting factor. In this review, the different therapeutic monoclonal antibodies directed against the microbial pathogens are discussed.
Insights
Monoclonal antibodies (mAbs) offer targeted, effective treatments for infectious diseases, addressing antimicrobial resistance. Advancements in mAb technology are crucial for managing viral outbreaks and bacterial infections, despite manufacturing costs.
Area of Science:
- Immunology
- Pharmacology
- Infectious Diseases
Background:
- Antimicrobial resistance necessitates novel therapeutic strategies.
- Monoclonal antibodies (mAbs) provide targeted pharmacotherapy with high specificity and efficacy.
- Conventional antimicrobials face challenges due to widespread resistance.
Purpose of the Study:
- To review therapeutic monoclonal antibodies (mAbs) targeting microbial pathogens.
- To highlight the role of mAbs in combating infectious diseases.
- To discuss advancements and challenges in mAb development for infectious conditions.
Main Methods:
- Review of approved and investigational monoclonal antibodies for infectious diseases.
- Discussion of current antibody engineering and production technologies.
- Analysis of the clinical applications and limitations of antimicrobial mAbs.
Main Results:
- Five mAbs are approved for infectious conditions: palivizumab (RSV), ibalizumab-uiyk (HIV-1), raxibacumab (anthrax), obiltoxaximab (anthrax), and bezlotoxumab (C. difficile).
- Approximately 30 viral and 15 bacterial mAbs are in development.
- Cutting-edge technologies enhance mAb production, but manufacturing cost remains a barrier.
Conclusions:
- Antimicrobial mAbs are essential alternatives and complements to conventional treatments.
- MAbs are particularly relevant for emerging viral outbreaks lacking vaccines.
- Continued innovation in mAb technology is vital for addressing global infectious disease challenges.
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