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

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Hybrid immunity to SARS-CoV-2 in patients with chronic lymphocytic leukemia. / Mellinghoff, Sibylle C; Robrecht, Sandra; Sprute, Rosanne; Mayer, Leonie; Weskamm, Leonie M; Dahlke, Christine; Gruell, Henning; Teipel, Finn; Schlößer, Hans A; Siepmann, Klara; Thelen, Martin; Fink, Anna-Maria; Fischer, Kirsten; Klein, Florian; Addo, Marylyn M; Kolovou, Androniki; Cornely, Oliver A; Eichhorst, Barbara; Hallek, Michael; Langerbeins, Petra.

In: EUR J HAEMATOL, Vol. 112, No. 5, 05.2024, p. 788-793.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Mellinghoff, SC, Robrecht, S, Sprute, R, Mayer, L, Weskamm, LM, Dahlke, C, Gruell, H, Teipel, F, Schlößer, HA, Siepmann, K, Thelen, M, Fink, A-M, Fischer, K, Klein, F, Addo, MM, Kolovou, A, Cornely, OA, Eichhorst, B, Hallek, M & Langerbeins, P 2024, 'Hybrid immunity to SARS-CoV-2 in patients with chronic lymphocytic leukemia', EUR J HAEMATOL, vol. 112, no. 5, pp. 788-793. https://doi.org/10.1111/ejh.14170

APA

Mellinghoff, S. C., Robrecht, S., Sprute, R., Mayer, L., Weskamm, L. M., Dahlke, C., Gruell, H., Teipel, F., Schlößer, H. A., Siepmann, K., Thelen, M., Fink, A-M., Fischer, K., Klein, F., Addo, M. M., Kolovou, A., Cornely, O. A., Eichhorst, B., Hallek, M., & Langerbeins, P. (2024). Hybrid immunity to SARS-CoV-2 in patients with chronic lymphocytic leukemia. EUR J HAEMATOL, 112(5), 788-793. https://doi.org/10.1111/ejh.14170

Vancouver

Bibtex

@article{5c1520f6f7a14df3876cc18d3a8d6f31,
title = "Hybrid immunity to SARS-CoV-2 in patients with chronic lymphocytic leukemia",
abstract = "OBJECTIVE: Preventing 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/RESULTS: Blood 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.CONCLUSION: Our 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.",
keywords = "Humans, SARS-CoV-2, Leukemia, Lymphocytic, Chronic, B-Cell/complications, COVID-19, COVID-19 Vaccines, Leukocytes, Mononuclear, Immunoglobulin G, Postoperative Complications, Vaccination, Adaptive Immunity, Antibodies, Viral",
author = "Mellinghoff, {Sibylle C} and Sandra Robrecht and Rosanne Sprute and Leonie Mayer and Weskamm, {Leonie M} and Christine Dahlke and Henning Gruell and Finn Teipel and Schl{\"o}{\ss}er, {Hans A} and Klara Siepmann and Martin Thelen and Anna-Maria Fink and Kirsten Fischer and Florian Klein and Addo, {Marylyn M} and Androniki Kolovou and Cornely, {Oliver A} and Barbara Eichhorst and Michael Hallek and Petra Langerbeins",
note = "{\textcopyright} 2024 The Authors. European Journal of Haematology published by John Wiley & Sons Ltd.",
year = "2024",
month = may,
doi = "10.1111/ejh.14170",
language = "English",
volume = "112",
pages = "788--793",
journal = "EUR J HAEMATOL",
issn = "0902-4441",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Hybrid immunity to SARS-CoV-2 in patients with chronic lymphocytic leukemia

AU - Mellinghoff, Sibylle C

AU - Robrecht, Sandra

AU - Sprute, Rosanne

AU - Mayer, Leonie

AU - Weskamm, Leonie M

AU - Dahlke, Christine

AU - Gruell, Henning

AU - Teipel, Finn

AU - Schlößer, Hans A

AU - Siepmann, Klara

AU - Thelen, Martin

AU - Fink, Anna-Maria

AU - Fischer, Kirsten

AU - Klein, Florian

AU - Addo, Marylyn M

AU - Kolovou, Androniki

AU - Cornely, Oliver A

AU - Eichhorst, Barbara

AU - Hallek, Michael

AU - Langerbeins, Petra

N1 - © 2024 The Authors. European Journal of Haematology published by John Wiley & Sons Ltd.

PY - 2024/5

Y1 - 2024/5

N2 - OBJECTIVE: Preventing 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/RESULTS: Blood 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.CONCLUSION: Our 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.

AB - OBJECTIVE: Preventing 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/RESULTS: Blood 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.CONCLUSION: Our 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.

KW - Humans

KW - SARS-CoV-2

KW - Leukemia, Lymphocytic, Chronic, B-Cell/complications

KW - COVID-19

KW - COVID-19 Vaccines

KW - Leukocytes, Mononuclear

KW - Immunoglobulin G

KW - Postoperative Complications

KW - Vaccination

KW - Adaptive Immunity

KW - Antibodies, Viral

U2 - 10.1111/ejh.14170

DO - 10.1111/ejh.14170

M3 - SCORING: Journal article

C2 - 38311570

VL - 112

SP - 788

EP - 793

JO - EUR J HAEMATOL

JF - EUR J HAEMATOL

SN - 0902-4441

IS - 5

ER -