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Immune response to conjugated meningococcal C vaccine in pediatric oncology patients
Joyce W Yu1, Astrid Borkowski, Lisa Danzig
1Division of Pediatric Allergy and Clinical Immunology, McGill University Health Centre, Montreal, Quebec, Canada.
Insights
Pediatric oncology patients showed varied responses to the Meningococcal C vaccine, with chemotherapy proximity and B cell count influencing effectiveness. Further research is needed to optimize vaccination strategies for immunocompromised children.
Area of Science:
- Immunology
- Pediatric Oncology
- Vaccinology
Background:
- Mass vaccination with Meningococcal CRM197 vaccine occurred in Quebec following disease outbreaks.
- Pediatric oncology patients undergoing chemotherapy or post-bone-marrow transplant were included in the study.
Purpose of the Study:
- To examine the immune response of pediatric oncology patients to the Meningococcal C vaccine.
- To identify factors influencing vaccine response in this vulnerable population.
Main Methods:
- An open-label, descriptive cohort study was conducted at the Montreal Children's Hospital.
- A positive vaccine response was defined by a fourfold increase in specific IgG and a human complement bactericidal assay (hBCA) titer >1:4.
Main Results:
- 13 of 25 patients with ALL showed a serologic response, with responders having higher B cell counts.
- Chemotherapy proximity was associated with non-response; only 2 of 5 post-bone-marrow transplant patients responded.
- 44% of patients achieved an adequate hBCA response, correlating significantly with serologic response.
Conclusions:
- Meningococcal C-conjugate vaccine elicits variable immune responses in pediatric cancer patients.
- Chemotherapy status and B cell count are potential predictors of vaccine response in this cohort.
Background:
Following outbreaks of meningococcal disease in Quebec in 1991-1993 and 2000-2001, a mass vaccination campaign was performed. In 2001-2002, children aged 2 months to 20 years were immunized with the Meningococcal CRM197 vaccine (Menjugate). We examined the response of pediatric oncology patients during or following maintenance chemotherapy and post-bone-marrow transplantation to Meningococcal C vaccine.
Procedure:
This was an open label descriptive study of a cohort of patients from the oncology clinic at the Montreal Children's Hospital. A positive vaccine response was defined as a fourfold increase in specific IgG from baseline and a bactericidal assay using human complement (hBCA) titer >1:4.
Results:
Of the 25 patients with ALL, 13 had a serologic response (average 60-fold increase). The serologic responders had a higher mean B cell count (0.262) compared to non-responders 0.068 x 10.9/L [t(23) = 2.843 (P < 0.05)]. Eleven of the 12 non-responders and 4 of the responders were on maintenance chemotherapy. In addition, two of the five patients post-bone-marrow transplant, responded. Fifteen of the 34 patients (44%) had an adequate hBCA response (mean titer 61). The group included 14/18 serologic responders with hBCA response (P < 0.001) and 16/17 non-serologic responders with no hBCA response (P < 0.001).
Conclusions:
Meningococcal C-conjugate vaccine produced variable responses in children with common cancers. Proximity to chemotherapy and total B cell number may help predict likelihood of response.
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