Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2023 Aug;19(2):2260040.
doi: 10.1080/21645515.2023.2260040. Epub 2023 Oct 6.

Respiratory delivery of passive immunotherapies for SARS-CoV-2 prophylaxis and therapy

Affiliations
Review

Respiratory delivery of passive immunotherapies for SARS-CoV-2 prophylaxis and therapy

Daniele Focosi et al. Hum Vaccin Immunother. 2023 Aug.

Abstract

Convalescent plasma has been extensively tested during the COVID-19 pandemic as a transfusion product. Similarly, monoclonal antibodies have been largely administered either intravenously or intramuscularly. Nevertheless, when used against a respiratory pathogen, respiratory delivery is preferable to maximize the amount of antibody that reaches the entry door in order to prevent sustained viral multiplication. In this narrative review, we review the different types of inhalation device and summarize evidence from animal models and early clinical trials supporting the respiratory delivery (for either prophylactic or therapeutic purposes) of convalescent plasma or monoclonal antibodies (either full antibodies, single-chain variable fragments, or camelid-derived monoclonal heavy-chain only antibodies). Preliminary evidences from animal models suggest similar safety and noninferior efficacy, but efficacy evaluation from clinical trials is still limited.

Keywords: COVID-19; Convalescent plasma; SARS-CoV-2; Spike; monoclonal antibodies; nasal immunotherapies; neutralizing antibodies; passive immunotherapies.

PubMed Disclaimer

Conflict of interest statement

No potential conflict of interest was reported by the author(s).

Figures

Figure 1.
Figure 1.
Potential approaches for respiratory delivery of passive immunotherapeutics against COVID-19.

Similar articles

Cited by

References

    1. Chavda VP, Baviskar KP, Vaghela DA, Raut SS, Bedse AP.. Nasal sprays for treating COVID-19: a scientific note. Pharmacol Rep. 2023;75(2):249–6. doi:10.1007/s43440-023-00463-7. - DOI - PMC - PubMed
    1. Parray HA, Shukla S, Perween R, Khatri R, Shrivastava T, Singh V, Murugavelu P, Ahmed S, Samal S, Sharma C, et al. Inhalation monoclonal antibody therapy: a new way to treat and manage respiratory infections. Appl Microbiol Biotechnol. 2021;105(16–17):6315–32. doi:10.1007/s00253-021-11488-4. - DOI - PMC - PubMed
    1. Ibañez LI, De Filette M, Hultberg A, Verrips T, Temperton N, Weiss RA, Vandevelde W, Schepens B, Vanlandschoot P, Saelens X, et al. Nanobodies with in vitro neutralizing activity protect mice against H5N1 influenza virus infection. J Infect Dis. 2011;203(8):1063–72. doi:10.1093/infdis/jiq168. - DOI - PubMed
    1. He F, Kumar SR, Syed Khader SM, Tan Y, Prabakaran M, Kwang J. Effective intranasal therapeutics and prophylactics with monoclonal antibody against lethal infection of H7N7 influenza virus. Antiviral Res. 2013;100(1):207–14. doi:10.1016/j.antiviral.2013.08.003. - DOI - PubMed
    1. Ye J, Shao H, Hickman D, Angel M, Xu K, Cai Y, Song H, Fouchier RAM, Qin A, Perez DR, et al. Intranasal delivery of an IgA monoclonal antibody effective against sublethal H5N1 influenza virus infection in mice. Clin Vaccine Immunol. 2010;17(9):1363–70. doi:10.1128/CVI.00002-10. - DOI - PMC - PubMed