Considerations for the development of monoclonal antibodies to address new viral variants in COVID-19

被引:0
作者
Casadevall, Arturo [1 ]
McConnell, Scott [1 ]
Focosi, Daniele [2 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Mol Microbiol & Immunol, Baltimore, MD 21205 USA
[2] Pisa Univ Hosp, North Western Tuscany Blood Bank, Pisa, Italy
关键词
Monoclonal antibodies; spike; COVID-19; SARS-CoV-2; immunocompromised; NEUTRALIZING ANTIBODY; HUMAN IGG1; EFFECTOR; AFFINITY; RECEPTOR; THERAPY; BINDING;
D O I
10.1080/14712598.2024.2388186
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
IntroductionMonoclonal antibody (mAb) therapies proved safe and effective in preventing progression of COVID-19 to hospitalization, but most were eventually defeated by continued viral evolution. mAb combinations and those mAbs that were deliberatively selected to target conserved regions of the SARS-CoV-2 spike protein proved more resilient to viral escape variants as evident by longer clinical useful lives.Areas coveredWe searched PubMed for literature covering the need, development, and use of mAb therapies for COVID-19. As much of humanity now has immunity to SARS-CoV-2, the population at most risk is that of immunocompromised individuals. Hence, there continues to be a need for mAb therapies for immunocompromised patients. However, mAb use in this population carries the risk for selecting mAb-resistant variants, which could pose a public health concern if they disseminate to the general population.Expert opinionGoing forward, structural knowledge of the interactions of Spike with its cellular receptor has identified several regions that may be good targets for future mAb therapeutics. A focus on designing variant-resistant mAbs together with cocktails that target several epitopes and the use of other variant mitigating strategies such as the concomitant use of small molecule antivirals and polyclonal preparations could extend the clinical usefulness of future preparations.
引用
收藏
页码:787 / 797
页数:11
相关论文
共 93 条
  • [1] A Neutralizing Monoclonal Antibody for Hospitalized Patients with Covid-19
    Lundgren J.D.
    Grund B.
    Barkauskas C.E.
    Holland T.L.
    Gottlieb R.L.
    Sandkovsky U.
    Brown S.M.
    Knowlton K.U.
    Self W.H.
    Files D.C.
    Jain M.K.
    Benfield T.
    Bowdish M.E.
    Leshnower B.G.
    Baker J.V.
    Jensen J.-U.
    Gardner E.M.
    Ginde A.A.
    Harris E.S.
    Johansen I.S.
    Markowitz N.
    Matthay M.A.
    Østergaard L.
    Chang C.C.
    Davey V.J.
    Goodman A.
    Higgs E.S.
    Murray D.D.
    Murray T.A.
    Paredes R.
    Parmar M.K.B.
    Phillips A.N.
    Reilly C.
    Sharma S.
    Dewar R.L.
    Teitelbaum M.
    Wentworth D.
    Cao H.
    Klekotka P.
    Babiker A.G.
    Gelijns A.C.
    Kan V.L.
    Polizzotto M.N.
    Thompson B.T.
    Lane H.C.
    Neaton J.D.
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2021, 384 (10) : 905 - 914
  • [2] Aleem A., 2023, MONOCLONAL ANTIBODY
  • [3] David versus goliath: ACE2-Fc receptor traps as potential SARS-CoV-2 inhibitors
    Alfaleh, Mohamed A.
    Zawawi, Ayat
    Al-Amri, Sawsan S.
    Hashem, Anwar M.
    [J]. MABS, 2022, 14 (01)
  • [4] Administration of Anti-SARS-CoV-2 Monoclonal Antibodies After US Food and Drug Administration Deauthorization
    Anderson, Timothy S.
    O'Donoghue, Ashley
    Mechanic, Oren
    Dechen, Tenzin
    Stevens, Jennifer
    [J]. JAMA NETWORK OPEN, 2022, 5 (08) : e2228997
  • [5] [Anonymous], 2024, Med Lett Drugs Ther, V66, P79, DOI 10.58347/tml.2024.1702e
  • [6] A perspective on potential antibody-dependent enhancement of SARS-CoV-2
    Arvin, Ann M.
    Fink, Katja
    Schmid, Michael A.
    Cathcart, Andrea
    Spreafico, Roberto
    Havenar-Daughton, Colin
    Lanzavecchia, Antonio
    Corti, Davide
    Virgin, Herbert W.
    [J]. NATURE, 2020, 584 (7821) : 353 - 363
  • [7] SARS-CoV-2 neutralizing antibody structures inform therapeutic strategies
    Barnes, Christopher O.
    Jette, Claudia A.
    Abernathy, Morgan E.
    Dam, Kim-Marie A.
    Esswein, Shannon R.
    Gristick, Harry B.
    Malyutin, Andrey G.
    Sharaf, Naima G.
    Huey-Tubman, Kathryn E.
    Lee, Yu E.
    Robbiani, Davide F.
    Nussenzweig, Michel C.
    West, Anthony P., Jr.
    Bjorkman, Pamela J.
    [J]. NATURE, 2020, 588 (7839) : 682 - +
  • [8] The anti-SARS-CoV-2 monoclonal antibody bamlanivimab minimally affects the endogenous immune response to COVID-19 vaccination
    Benschop, Robert J.
    Tuttle, Jay L.
    Zhang, Lin
    Poorbaugh, Josh
    Kallewaard, Nicole L.
    Vaillancourt, Peter
    Crisp, Melissa
    Thi Ngoc Vy Trinh
    Freitas, Joshua J.
    Beasley, Stephanie
    Daniels, Montanea
    Haustrup, Natalie
    Higgs, Richard E.
    Nirula, Ajay
    Cohen, Myron S.
    Marovich, Mary
    [J]. SCIENCE TRANSLATIONAL MEDICINE, 2022, 14 (655)
  • [9] Intravenous immunoglobulins for the treatment of prolonged COVID-19 in immunocompromised patients: a brief report
    Billi, Benedicte
    Cholley, Paul
    Grobost, Vincent
    Clement, Melissa
    Rieu, Virginie
    Le Guenno, Guillaume
    Lobbes, Herve
    [J]. FRONTIERS IN IMMUNOLOGY, 2024, 15
  • [10] Anti-Spike Monoclonal Antibody Monotherapies and Immune Escape Risk Minimization Strategies
    Casadevall, Arturo
    Focosi, Daniele
    [J]. CLINICAL INFECTIOUS DISEASES, 2024, 80 (02) : 484 - 485