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Expanding Cytotoxic T Lymphocytes from Umbilical Cord Blood that Target Cytomegalovirus, Epstein-Barr Virus, and Adenovirus
Published on: May 7, 2012
Cytomegalovirus disease in children with acute lymphoblastic leukemia
Richa Jain1, Amita Trehan1, Baijyantimala Mishra2
1a Division of Pediatric Hematology and Oncology, Department of Pediatrics , Advanced Pediatric Centre, Postgraduate Institute of Medical Education and Research , Chandigarh , India.
Insights
Cytomegalovirus (CMV) significantly impacts children with acute lymphoblastic leukemia (ALL) undergoing chemotherapy, causing fever and organ damage. Early detection and treatment with ganciclovir improve outcomes for these vulnerable patients.
Area of Science:
- Pediatric Oncology
- Infectious Diseases
- Hematology
Background:
- Viral infections, particularly cytomegalovirus (CMV), are often overlooked in pediatric acute lymphoblastic leukemia (ALL) patients receiving chemotherapy.
- High CMV seroprevalence in regions like India suggests it's a critical pathogen causing fever, cytopenia, and end-organ damage in this population.
- Limited data exist on CMV disease incidence and presentation in pediatric ALL.
Purpose of the Study:
- To prospectively evaluate the incidence and clinical manifestations of CMV disease in children with ALL and prolonged febrile neutropenia (FN).
- To assess the role of CMV as a pathogen in pediatric ALL patients experiencing prolonged FN or end-organ damage.
- To identify factors associated with CMV infection and recurrence in this cohort.
Main Methods:
- Prospective assessment of pediatric ALL patients with prolonged FN over 3 years for CMV disease.
- Evaluation of patients with end-organ damage (pneumonia, retinitis, colitis) for CMV involvement.
- Utilized quantitative and qualitative PCR from various samples (blood, body fluids, tissue) and ophthalmologic examinations.
Main Results:
- CMV disease was detected in 10% of pediatric ALL patients with prolonged FN.
- CMV infection was also identified in patients with end-organ damage, commonly affecting the lungs and eyes.
- CMV reactivation frequently occurred during less intensive chemotherapy phases; prolonged lymphopenia correlated with infection relapse.
Conclusions:
- Cytomegalovirus is a significant pathogen in children undergoing standard chemotherapy for ALL.
- Early diagnosis and targeted antiviral therapy, such as parenteral ganciclovir for 14-21 days, lead to favorable outcomes and prevent recurrence.
- Monitoring for CMV is crucial in pediatric ALL patients, especially those with prolonged FN or lymphopenia.
Abstract:
Viral infections are an underrecognized problem in children on standard chemotherapy for acute lymphoblastic leukemia (ALL). In countries with high baseline seroprevalence of cytomegalovirus (CMV) such as India, it may be an important pathogen leading to fever, end-organ damage, and cytopenia. Data regarding the incidence and manifestations of CMV disease in pediatric ALL patients are scanty. The authors prospectively assessed all children on chemotherapy for ALL with prolonged febrile neutropenia (FN) for CMV disease over a 3-year period. Children with end-organ damage, including pneumonia, retinitis, and colitis, were also evaluated. Quantitative and qualitative polymerase chain reaction (PCR) from blood, body fluids, or tissue was done along with ophthalmologic evaluation. CMV disease was detected in 10% of the children with prolonged FN. In addition, other children were identified due to end-organ damage, lung and eye being the common organs of involvement. Time of CMV reactivation was essentially during nonintense phase of chemotherapy. Lymphopenia was present in most children, and prolonged lymphopenia was associated with relapse of CMV infection after therapy. The authors conclude that CMV is an important pathogen in children on standard chemotherapy for ALL. It has a good outcome with early detection and directed therapy. Parenteral ganciclovir is needed for a period of 14-21 days to prevent recurrence.
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