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Immunity to and infant mortality from measles
Summary
Infant measles mortality is unlikely due to immunodeficiency. Most immune responses to measles were similar between infants and older children, with younger infants showing better prognostic indicators.
Area of Science:
- Immunology
- Pediatrics
- Infectious Diseases
Background:
- High infant mortality from infectious diseases necessitates understanding age-related immune responses.
- Measles infection presents a significant risk to infants, prompting investigation into underlying immune factors.
Purpose of the Study:
- To investigate the age-related immune response to natural measles infection.
- To determine if immunodeficiency contributes to high infant mortality rates from measles.
Main Methods:
- Compared immune responses in infants (<12 months) and older children (>12 months) over 6 weeks post-measles rash onset.
- Assessed lymphocyte transformation, antibody titers (complement-fixing, haemagglutination inhibition), immunoglobulin levels (IgG, IgM, IgA), complement components (C3, C4, Factor B), total hemolytic complement, alternative complement pathway, and leukocyte migration inhibition.
Main Results:
- No significant differences in most immunological parameters between younger and older children.
- Younger infants (group A) had higher absolute lymphocyte counts and haemagglutination inhibition antibody levels, and lower C4 levels compared to older children (group B).
- Five deaths occurred, all in infants under 15 months, but observed immunological differences favored a better prognosis in the younger group.
Conclusions:
- The high mortality rate in infants from measles is unlikely attributable to immunodeficiency.
- Observed immunological differences in younger infants suggest factors other than immunodeficiency are at play.
- Immune responses to measles are largely not age-dependent in the studied parameters.