Hybrid immunity to SARS‐CoV‐2 in patients with chronic lymphocytic leukemia

Author:

Mellinghoff Sibylle C.123ORCID,Robrecht Sandra1ORCID,Sprute Rosanne12,Mayer Leonie456ORCID,Weskamm Leonie M.456ORCID,Dahlke Christine456ORCID,Gruell Henning27ORCID,Teipel Finn27ORCID,Schlößer Hans A.8ORCID,Siepmann Klara8,Thelen Martin8ORCID,Fink Anna‐Maria1ORCID,Fischer Kirsten1,Klein Florian267,Addo Marylyn M.4569ORCID,Kolovou Androniki12ORCID,Cornely Oliver A.12310ORCID,Eichhorst Barbara1ORCID,Hallek Michael1ORCID,Langerbeins Petra1ORCID

Affiliation:

1. Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Center for Integrated Oncology Aachen Bonn Cologne Duesseldorf (CIO ABCD) and Excellence Center for Medical Mycology (ECMM) University of Cologne Cologne Germany

2. German Centre for Infection Research (DZIF), Partner Site Bonn‐Cologne Cologne Germany

3. Faculty of Medicine and University Hospital Cologne, Institute of Translational Research, Cologne Excellence Cluster on Cellular Stress Responses in Aging‐Associated Diseases (CECAD) University of Cologne Cologne Germany

4. Department of Clinical Immunology of Infectious Diseases Bernhard Nocht Institute for Tropical Medicine Hamburg Germany

5. Institute for Infection Research and Vaccine Development (IIRVD) University Medical Centre Hamburg‐Eppendorf Hamburg Germany

6. German Centre for Infection Research (DZIF), Partner Site Hamburg‐Lübeck‐Borstel‐Riems Hamburg Germany

7. Institute of Virology, Faculty of Medicine and University Hospital Cologne University of Cologne Cologne Germany

8. Faculty of Medicine and University Hospital Cologne Center for Molecular Medicine Cologne, University of Cologne Cologne Germany

9. Division of Infectious Diseases, First Department of Medicine University Medical Centre Hamburg‐Eppendorf Hamburg Germany

10. Faculty of Medicine and University Hospital Cologne, Clinical Trials Centre Cologne (ZKS Köln) University of Cologne Cologne Germany

Abstract

AbstractObjectivePreventing severe COVID‐19 remains a priority globally, particularly in the immunocompromised population. As shown in healthy individuals, immunity against SARS‐CoV‐2 can be yielded by previous infection, vaccination, or both (hybrid immunity). The objective of this observation study was to investigate hybrid immunity in patients with chronic lymphocytic leukemia (CLL).Methods/ResultsBlood samples of six patients with CLL were collected 55 days after fourth COVID‐19 vaccination. All patients had a SARS‐CoV‐2 infection within 12 months before the second booster (fourth vaccination). SARS‐CoV‐2 spike receptor binding domain (RBD)‐specific IgG antibodies were detectable in 6/6 (100.0%) CLL patients after four compared to 4/6 (66.7%) after three vaccinations. The median number of SARS‐CoV‐2 spike‐specific T cells after repeated booster vaccination plus infection was 166 spot‐forming cells (SFC) per million peripheral blood mononuclear cells. Overall, 5/5 (100%) studied patients showed a detectable increase in T cell activity.ConclusionOur data reveal an increase of cellular and humoral immune response in CLL patients after fourth COVID‐19 vaccination combined with SARS‐CoV‐2 infection, even in those undergoing B cell‐depleting treatment. Patients with prior vaccination failure now show a specific IgG response. Future research should explore the duration and effectiveness of hybrid immunity considering various factors like past infection and vaccination rates, types and numbers of doses, and emerging variants.

Publisher

Wiley

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