COVA1-18 neutralizing antibody protects against SARS-CoV-2 in three preclinical models.
Pauline MaisonnasseYoann AldonAurélien MarcRomain MarlinNathalie BosquetNatalia A KuzminaAlec W FreynJonne L SnitselaarAntonio GonçalvesTom G CanielsJudith A BurgerMeliawati PonimanIlja BontjerVirginie ChesnaisSégolène DiryAnton IershovAdam J RonkSonia JangraRaveen RathnasinghePhilip J M BrouwerTom P L BijlJelle van SchootenMitch BrinkkemperHejun LiuMeng YuanChad E MireMariëlle J van BreemenVanessa ContrerasThibaut NaninckJulien LemaîtreNidhal KahlaouiFrancis RelouzatCatherine ChaponRaphaël Ho Tsong FangCharlene McDanalMary Osei-TwumNatalie St-AmantLuc GagnonDavid C MontefioriIan A WilsonEric GinouxGodelieve J de BreeAdolfo García-SastreMichael SchotsaertLynda CoughlanAlexander BukreyevSylvie van der WerfJeremie GuedjRogier W SandersMarit J van GilsRoger Le GrandPublished in: Nature communications (2021)
Effective treatments against Severe Acute Respiratory Syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Monoclonal antibodies have shown promising results in patients. Here, we evaluate the in vivo prophylactic and therapeutic effect of COVA1-18, a neutralizing antibody highly potent against the B.1.1.7 isolate. In both prophylactic and therapeutic settings, SARS-CoV-2 remains undetectable in the lungs of treated hACE2 mice. Therapeutic treatment also causes a reduction in viral loads in the lungs of Syrian hamsters. When administered at 10 mg kg-1 one day prior to a high dose SARS-CoV-2 challenge in cynomolgus macaques, COVA1-18 shows very strong antiviral activity in the upper respiratory compartments. Using a mathematical model, we estimate that COVA1-18 reduces viral infectivity by more than 95% in these compartments, preventing lymphopenia and extensive lung lesions. Our findings demonstrate that COVA1-18 has a strong antiviral activity in three preclinical models and could be a valuable candidate for further clinical evaluation.