2020
DOI: 10.3390/cells9112398
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Chronic Lymphocytic Leukemia-Induced Humoral Immunosuppression: A Systematic Review

Abstract: Secondary immunodeficiency is observed in all patients with chronic lymphocytic leukemia (CLL) in varying degrees. The aim of the study was to review the available literature data on patients with CLL, with particular regard to the pathogenesis of the disease and the impact of humoral immunity deficiency on the clinical and therapeutic approach. A systematic literature review was carried out by two independent authors who searched PubMed databases for studies published up to January 2020. Additionally, Google … Show more

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Cited by 12 publications
(8 citation statements)
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“… 43 , 51 , 55 , 56 , 57 The clinical and molecular heterogeneity of CLL patients is well‐known. 58 Since the production of antibodies against the S protein depends on proper T and B cell interaction, both quantitative and qualitative humoral and cellular defects in immune cells reduce response to vaccines.…”
Section: Patients With Cll As the Population At A High Risk Of Non‐response To Covid‐19 Vaccinementioning
confidence: 99%
“… 43 , 51 , 55 , 56 , 57 The clinical and molecular heterogeneity of CLL patients is well‐known. 58 Since the production of antibodies against the S protein depends on proper T and B cell interaction, both quantitative and qualitative humoral and cellular defects in immune cells reduce response to vaccines.…”
Section: Patients With Cll As the Population At A High Risk Of Non‐response To Covid‐19 Vaccinementioning
confidence: 99%
“…The role for Ig treatment in the present case cannot be determined definitely. However, several reports indicate that substitution of Ig improves the outcome of severe infections in CLL patients and humoral immune deficiencies despite normal IgG and IgM serum levels have been described [8,9,14,15].…”
Section: Discussionmentioning
confidence: 99%
“…The occurrence of reduced gammaglobulinemia in CLL patients is more marked with advanced-stage disease and linked with patient age and associated pathologies (91). This occurs in CLL subjects with mutated and unmutated immunoglobulin heavy chain genes (99)(100)(101).…”
Section: Characteristics Of Secondary Immunodeficiency In Patients With Chronic Lymphocytic Leukemiamentioning
confidence: 99%