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1.
Br J Haematol ; 202(3): 498-503, 2023 08.
Artigo em Inglês | MEDLINE | ID: mdl-37303189

RESUMO

Limited data exist on COVID-19 vaccination efficacy in patients with acute myeloid leukemia and myelodysplasia with excess blasts (AML/MDS-EB2). We report results from a prospective study, PACE (Patients with AML and COVID-19 Epidemiology). 93 patients provided samples post-vaccine 2 or 3 (PV2, PV3). Antibodies against SARS-COV-2 spike antigen were detectable in all samples. Neutralization of the omicron variant was poorer than ancestral variants but improved PV3. In contrast, adequate T-cell reactivity to SARS-COV-2 spike protein was seen in only 16/47 (34%) patients PV2 and 23/52 (44%) PV3. Using regression models, disease response (not in CR/Cri), and increasing age predicted poor T cell response.


Assuntos
COVID-19 , Leucemia Mieloide Aguda , Síndromes Mielodisplásicas , Humanos , Vacinas contra COVID-19 , Estudos Prospectivos , Linfócitos T , COVID-19/prevenção & controle , SARS-CoV-2 , Leucemia Mieloide Aguda/terapia , Síndromes Mielodisplásicas/terapia , Vacinação , Anticorpos Antivirais
2.
Case Rep Hematol ; 2017: 5762525, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-29201472

RESUMO

Clinically significant cytomegalovirus (CMV) reactivation is not uncommon in patients with severe immunodeficiency secondary to underlying medical disorders or following aggressive immunosuppressive therapy. However, it is less frequently found in patients with low-grade haematological malignancies after nonintensive chemotherapy. We treated a patient at our centre for stage IVB follicular lymphoma with standard chemotherapy who successively developed CMV colitis associated with a CMV viral load of >3 million copies/ml. Four lines of antiviral treatment were necessary to obtain biochemical remission with undetectable CMV levels, with an initially insufficient response to valganciclovir despite therapeutic pre- and posttreatment levels. Subsequently, our patient also developed an infection with Pneumocystis jirovecii pneumonia (PJP) as further evidence of severe immune compromise. This case report demonstrates the importance of including investigations for less common sources of infection when confronted with a patient with a low-grade haematological malignancy and a pyrexia of unknown origin.

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