2022
DOI: 10.1016/j.coviro.2022.101204
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Monoclonal antibodies against rabies: current uses in prophylaxis and in therapy

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Cited by 37 publications
(35 citation statements)
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“…Due to the global shortage and high price of HRIG, WHO recommended the use of mAbs as alternatives for RIG in PEP, and to date, several mAbs have been approved or are in clinical trials 43–45 . As an integral part of PEP where vaccination usually takes time to induce an immune response, passive immunization of anti‐RABV mAbs could neutralize RABV and lyse infected cells by ADCC immediately after RABV exposure.…”
Section: Discussionmentioning
confidence: 99%
“…Due to the global shortage and high price of HRIG, WHO recommended the use of mAbs as alternatives for RIG in PEP, and to date, several mAbs have been approved or are in clinical trials 43–45 . As an integral part of PEP where vaccination usually takes time to induce an immune response, passive immunization of anti‐RABV mAbs could neutralize RABV and lyse infected cells by ADCC immediately after RABV exposure.…”
Section: Discussionmentioning
confidence: 99%
“…Compared wtih polyclonal products, Palivizumab provides an increased batch-to-batch stability and a reduced risk of blood-borne pathogen infection with approximately 50-fold enhanced potency (Graham and Ambrosino, 2015). These advantages are also the reasons why mAb drugs are replacing polyclonal antibody products against rabies virus (de Melo et al, 2022), HBV (Cerino et al, 2019) and other pathogens or toxins. Overall, achievements in bioscience, medical science, and bioengineering have accelerated the clinical development of antibody drugs targeting TNF-α, EGFR, CD20, HER2, PD-1/PD-L1 and emerging new molecules (Carter and Lazar, 2018).…”
Section: Introductionmentioning
confidence: 99%
“…Therefore, the use of monoclonal antibody (mAb) to prevent or treat virus-induced infectious diseases is a clear and well-reasoned clinical strategy. This year’s Antiviral Strategies section of Current Opinion in Virology updates the research and development of mAbs against a number of important viruses, including human immunodeficiency virus (HIV) [1] , Ebola virus (EBOV) [2] , Hepatitis B virus (HBV) [3] , influenza virus [4] , coronavirus [5] , human cytomegalovirus (HCMV) [6] , and rabies virus [7] . Moreover, the development of a plant-based platform for producing mAbs against viral infections is also reviewed [8] .…”
mentioning
confidence: 99%
“…HCMV, with a very broad cell tropism, has multiple surface GPs targeting distinct host receptors, while mAbs against these viral GPs (gB, gM/gN complex, gH/gL/gO trimer, and gH/gL/pUL128/130/131 pentamer) are neutralizing [6] . Rabies G protein on the surface of the viral particles, with its ectodomain stabilized by several disulfide bonds, has six antigenic sites (I, IIa, IIb, III, IV, and ‘a’) and is the main target for antirabies neutralizing antibodies [7] . In conclusion, characterization of the Fab region of natural antibodies revealed various neutralizing epitopes on the viral surface proteins and facilitate the elucidation of the molecular mechanisms for neutralization.…”
mentioning
confidence: 99%
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