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Updated: Aug 17, 2026

Bone Marrow-derived Macrophage Production
Published on: November 22, 2013
Role of macrophages in host resistance to group A streptococci
Oliver Goldmann1, Manfred Rohde, Gursharan Singh Chhatwal
1Department of Microbial Pathogenesis and Vaccine Research, GBF-German Research Centre for Biotechnology, Braunschweig, Germany.
Abstract:
Macrophages provide the first line of defense against invading pathogens. The aim of this study was to determine the role of macrophages during infection with group A streptococci (Streptococcus pyogenes) in mice. Here, we report that resident macrophages can efficiently take up and kill S. pyogenes during in vivo infection, as demonstrated by immunofluorescence and electron microscopy, as well as colony counts. To evaluate the contribution of macrophages to the resolution of experimental infection with S. pyogenes, we compared the susceptibility of BALB/c mice rendered macrophage deficient by treatment with carrageenan with that of intact mice. The results show that depletion of macrophages enhanced the susceptibility of BALB/c mice to S. pyogenes infection, as evidenced by 100% mortality of macrophage-depleted mice compared to 90% survival of nondepleted control animals. The in vivo depletion of macrophages strongly enhanced bacterial loads in the blood and systemic organs. Resistance to S. pyogenes can be restored in macrophage-depleted mice by adoptive transfer of purified macrophages. The in vivo blocking of the macrophage phagocytic function by treatment with gadolinium III chloride also resulted in enhanced susceptibility to S. pyogenes. Interestingly, depletion of macrophages prior to or during the first 24 h of infection decreased survival dramatically; in contrast, no mortality was observed in infected nondepleted animals or mice depleted after 48 h of infection. These results emphasize the important contribution of macrophages to the early control of S. pyogenes infection.
Insights
Macrophages are crucial for early defense against Streptococcus pyogenes. Depleting macrophages significantly increases mortality and bacterial load, highlighting their essential role in controlling this infection.
Area of Science:
- Immunology
- Microbiology
- Infectious Diseases
Background:
- Macrophages are key immune cells providing the first line of defense against pathogens.
- Group A Streptococcus (Streptococcus pyogenes) is a significant human pathogen requiring effective immune control.
Purpose of the Study:
- To elucidate the role of macrophages in host defense against Streptococcus pyogenes infection in a murine model.
- To determine the impact of macrophage depletion and functional impairment on S. pyogenes pathogenesis.
Main Methods:
- Utilized carrageenan to induce macrophage deficiency in BALB/c mice.
- Employed immunofluorescence, electron microscopy, and colony counts to assess bacterial burden and macrophage activity.
- Investigated the effect of gadolinium III chloride on macrophage phagocytic function in vivo.
- Assessed survival rates and bacterial dissemination in macrophage-depleted versus control mice.
Main Results:
- Resident macrophages efficiently phagocytosed and killed S. pyogenes in vivo.
- Macrophage depletion led to 100% mortality and increased bacterial loads in blood and organs.
- Adoptive transfer of macrophages restored resistance in depleted mice.
- Inhibition of macrophage phagocytosis increased susceptibility to infection.
- Early macrophage depletion (within 24h) was critical for survival, while later depletion had less impact.
Conclusions:
- Macrophages play a vital role in the early control and resolution of Streptococcus pyogenes infections.
- Maintaining macrophage function is essential for preventing severe disease and mortality during S. pyogenes infection.
- Targeting macrophages could be a potential therapeutic strategy for severe streptococcal infections.
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