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Treatment of chronic or relapsing COVID-19 in immunodeficiency - 03/02/22

Doi : 10.1016/j.jaci.2021.10.031 
Li-An K. Brown, MRCP a, b, Ed Moran, PhD c, Anna Goodman, DPhil d, Helen Baxendale, PhD e, William Bermingham, MBBS f, Matthew Buckland, PhD g, h, Iman AbdulKhaliq, MBBS i, Hannah Jarvis, MBBS j, Michael Hunter, FRCP k, Surendra Karanam, FRCPath l, Aisha Patel, MBBS b, Megan Jenkins, MBBS c, Alexander Robbins, MBBS m, Sujoy Khan, FRCPath n, Thomas Simpson, MBBS o, Stephen Jolles, MD, PhD p, Jonathan Underwood, PhD q, r, Sinisa Savic, PhD s, t, Alex Richter, MD f, u, Adrian Shields, PhD f, u, Michael Brown, PhD b, v, David M. Lowe, PhD a, j,
a Institute of Immunity and Transplantation, University College London, London, United Kingdom 
b University College London Hospital NHS Foundation Trust, London, United Kingdom 
c North Bristol NHS Trust, Bristol, United Kingdom 
d Guy’s and St. Thomas’ NHS Foundation Trust, London, United Kingdom 
e Royal Papworth Hospital NHS Foundation Trust, Cambridge, United Kingdom 
f University Hospitals Birmingham NHS Foundation Trust, Birmingham, United Kingdom 
g Barts Health, London, United Kingdom 
h Institute of Child Health, University College London and Great Ormond Street Hospital, London, United Kingdom 
i Mid and South Essex NHS Foundation Trust, Essex, United Kingdom 
j Royal Free London NHS Foundation Trust, London, United Kingdom 
k Royal Victoria Hospital, Belfast, United Kingdom 
l Sandwell and West Birmingham Hospitals NHS Trust, Birmingham, United Kingdom 
m Imperial College Healthcare NHS Trust, London, United Kingdom 
n Hull University Teaching Hospitals NHS Trust, Hull, United Kingdom 
o Lewisham and Greenwich NHS Trust, London, United Kingdom 
p University Hospital of Wales, Cardiff, United Kingdom 
q Department of Infectious Diseases, Cardiff and Vale University Health Board, Cardiff, United Kingdom 
r Division of Infection and Immunity, Cardiff University, Cardiff, United Kingdom 
s Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom 
t Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom 
u Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, United Kingdom 
v Clinical Research Department, London School of Hygiene and Tropical Medicine, London, United Kingdom 

Corresponding author: David M. Lowe, PhD, Institute of Immunity and Transplantation, University College London, Royal Free Campus, Pond Street, London, NW3 2QG.Institute of Immunity and TransplantationUniversity College LondonRoyal Free CampusPond StreetLondonNW3 2QG

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Abstract

Background

Patients with some types of immunodeficiency can experience chronic or relapsing infection with severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). This leads to morbidity and mortality, infection control challenges, and the risk of evolution of novel viral variants. The optimal treatment for chronic coronavirus disease 2019 (COVID-19) is unknown.

Objective

Our aim was to characterize a cohort of patients with chronic or relapsing COVID-19 disease and record treatment response.

Methods

We conducted a UK physician survey to collect data on underlying diagnosis and demographics, clinical features, and treatment response of immunodeficient patients with chronic (lasting ≥21 days) or relapsing (≥2 episodes) of COVID-19.

Results

We identified 31 patients (median age 49 years). Their underlying immunodeficiency was most commonly characterized by antibody deficiency with absent or profoundly reduced peripheral B-cell levels; prior anti-CD20 therapy, and X-linked agammaglobulinemia. Their clinical features of COVID-19 were similar to those of the general population, but their median duration of symptomatic disease was 64 days (maximum 300 days) and individual patients experienced up to 5 episodes of illness. Remdesivir monotherapy (including when given for prolonged courses of ≤20 days) was associated with sustained viral clearance in 7 of 23 clinical episodes (30.4%), whereas the combination of remdesivir with convalescent plasma or anti-SARS-CoV-2 mAbs resulted in viral clearance in 13 of 14 episodes (92.8%). Patients receiving no therapy did not clear SARS-CoV-2.

Conclusions

COVID-19 can present as a chronic or relapsing disease in patients with antibody deficiency. Remdesivir monotherapy is frequently associated with treatment failure, but the combination of remdesivir with antibody-based therapeutics holds promise.

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Key words : COVID-19, SARS-CoV-2, immunodeficiency, therapeutic monoclonal, remdesivir

Abbreviations used : COVID-19, CRP, CVID, SARS-CoV-2, XLA


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 Disclosure of potential conflict of interest: T. Simpson has received speakers’ fees from Gilead. S. Jolles reports advisory board, speaker, conference, drug safety monitoring board, and project support from CSL Behring, Shire, Takeda, BioCryst Pharmaceuticals, Swedish Orphan Biovitrum, Biotest, Binding Site, LFB, Octapharma, Grifols, UCB Pharma, Sanofi, Pharming, Weatherden, and Zarodex Therapeutics, Limited, and he is a member of the IPOPI SAFE Taskforce and COVIC19 Trial Group. M. Brown is the UK chief investigator for a Gilead remdesivir trial (GS-US-540-9012), local principal investigator for a Gilead remdesivir trial (GS-US-540-5773/5774), and local coinvestigator for the AstraZeneca PROVENT trial. D. Lowe has received travel and subsistence costs for consultancy work for CSL Behring and fees for roundtable discussion from Merck; in addition, he is chief investigator for the COVID-19 antiviral FLARE trial (NCT04499677), and he holds research grants from LifeArc, the UK Medical Research Council, Blood Cancer UK, Bristol-Myers Squibb and the British Society for Antimicrobial Chemotherapy. The rest of the authors declare that they have no relevant conflicts of interest.


© 2021  American Academy of Allergy, Asthma & Immunology. Pubblicato da Elsevier Masson SAS. Tutti i diritti riservati.
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P. 557 - Febbraio 2022 Ritorno al numero
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