Hyper-Enriched Anti-RSV Immunoglobulins Nasally Administered: A Promising Approach for Respiratory Syncytial Virus Prophylaxis.


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
Historique:
received: 22 03 2021
accepted: 17 05 2021
entrez: 24 6 2021
pubmed: 25 6 2021
medline: 6 7 2021
Statut: epublish

Résumé

Respiratory syncytial virus (RSV) is a public health concern that causes acute lower respiratory tract infection. So far, no vaccine candidate under development has reached the market and the only licensed product to prevent RSV infection in at-risk infants and young children is a monoclonal antibody (Synagis Respiratory Syncytial Virus (RSV) is the major cause of acute lower respiratory infections in children, and is also recognized as a cause of morbidity in the elderly. There are still no vaccines and no efficient antiviral therapy against this virus. Here, we described an approach of passive immunization with a new class of hyper-enriched anti-RSV immunoglobulins (Ig) manufactured from human normal plasma. This new class of immunoglobulin plasma derived product is generated by an innovative bioprocess, called Ig cracking, which requires a combination of expertise in both plasma derived products and affinity chromatography. The strong efficacy in a small volume of these hyper-enriched anti-RSV IgG to inhibit the viral infection was demonstrated using a mouse model. This new class of immunoglobulin plasma-derived products could be applied to other pathogens to address specific therapeutic needs in the field of infectious diseases or even pandemics, such as COVID-19.

Identifiants

pubmed: 34163482
doi: 10.3389/fimmu.2021.683902
pmc: PMC8215542
doi:

Substances chimiques

Antibodies, Viral 0
F protein, human respiratory syncytial virus 0
Immunoglobulin G 0
Viral Fusion Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

683902

Informations de copyright

Copyright © 2021 Jacque, Chottin, Laubreton, Nogre, Ferret, de Marcos, Baptista, Drajac, Mondon, De Romeuf, Rameix-Welti, Eléouët, Chtourou, Riffault, Perret and Descamps.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Emilie Jacque (E)

LFB Biotechnologies, Les Ulis, France.

Claire Chottin (C)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Daphné Laubreton (D)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Michel Nogre (M)

LFB Biotechnologies, Les Ulis, France.

Cécile Ferret (C)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Sandrine de Marcos (S)

LFB Biotechnologies, Les Ulis, France.

Linda Baptista (L)

LFB Biotechnologies, Les Ulis, France.

Carole Drajac (C)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Philippe Mondon (P)

LFB Biotechnologies, Les Ulis, France.

Christophe De Romeuf (C)

LFB Biotechnologies, Les Ulis, France.

Marie-Anne Rameix-Welti (MA)

Université Paris-Saclay, UVSQ, Inserm, Infection et inflammation, U1173, Montigny-Le-Bretonneux, France.
AP-HP, Hôpital Ambroise Paré, Laboratoire de Microbiologie, Boulogne-Billancourt, France.

Jean-François Eléouët (JF)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Sami Chtourou (S)

LFB Biotechnologies, Les Ulis, France.

Sabine Riffault (S)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

Gérald Perret (G)

LFB Biotechnologies, Les Ulis, France.

Delphyne Descamps (D)

Université Paris-Saclay, INRAE, UVSQ, VIM, Jouy-en-Josas, France.

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Classifications MeSH