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Published on: April 5, 2019
THE THERAPEUTIC VALUE OF INTRAMUSCULAR DOSAGE OF TYPE I PNEUMOCOCCUS ANTISERA
1Department of Pathology, University and Bellevue Hospital Medical College and the Simon Baruch Foundation for Research in Pneumonia, and the Bureau of Laboratories, Department of Health of the City of New York, New York.
Intramuscular administration of antipneumococcus serum is as effective as intravenous delivery for treating pneumococcal infections in rabbits, especially in less severe cases. This suggests intramuscular serum may be a viable option for human pneumonia treatment.
Area of Science:
- Immunology
- Infectious Diseases
- Pharmacology
Background:
- Pneumococcal infections pose a significant public health challenge.
- Antipneumococcus sera are crucial in treating severe bacterial infections.
- Intravenous administration is the standard route for serum therapy.
Purpose of the Study:
- To compare the efficacy of intramuscular versus intravenous administration of antipneumococcus sera.
- To evaluate the bactericidal effects of different serum administration routes.
- To assess the potential of intramuscular serum delivery for human lobar pneumonia.
Main Methods:
- Rabbits with induced dermal pneumococcic infections were used as a model.
- Serum efficacy was assessed based on infection outcomes and bactericidal effects.
- Bloodstream invasion levels were considered in the analysis.
Main Results:
- Intramuscular antipneumococcus sera demonstrated comparable efficacy to intravenous dosage in rabbits with standard infections.
- The immediate bactericidal effect was equivalent between intramuscular and intravenous routes for mild to moderate bacteremias.
- Efficacy was maintained provided bloodstream invasion was not unusually high.
Conclusions:
- Intramuscular serum administration is a potentially effective alternative to intravenous delivery for pneumococcal infections.
- The findings support further investigation into intramuscular serum therapy for human lobar pneumonia.
- A controlled clinical trial is recommended to validate these results in human patients.
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