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Monitoring Immune Cells Trafficking Fluorescent Prion Rods Hours after Intraperitoneal Infection
Published on: November 19, 2010
Abstract:
The evidence summarized in this article is sufficient to support conclusions as follows. 1) Antibiotics penetrate rapidly into mammalian cells and inhibit multiplication of susceptible microbes within the cell as promptly and effectively as they inhibit multiplication of such microbes outside the cell. This is consistent with clinical experience. 2) Death of individual organisms inside mammalian cells bathed in medium containing antibiotics continues over several weeks but may not proceed pari passu with time. This observation supports the as yet meager clinical data, which suggest that eradication of the typhoid carrier state may be accomplished through antibiotic therapy, provided (i) the proper antibiotic is selected; (ii) it is administered in amounts sufficient to obtain continuous suppression of growth of intracellular organisms; and (iii) the regimen is maintained for 2 or 3 weeks. 3) The actual cause of death and destruction of intracellular microbes in treated cells remains an enigma. To attribute this to inanition or senescence of the organisms, without describing mechanisms, is to avoid the issue. The hypotheses dealing with inactivation of intracellular microbes by intracellular antimicrobial substances and antibodies deserve to be explored. 4) Evidence from the ward and laboratory suggests that infected cells can clear themselves of invading pathogens and recover. Although antibiotics have played the major role in demonstrating this in the laboratory, it is possible that they do nothing more than hold the intruders in abeyance while natural defense mechanisms of the cell gain the upper hand. Certainly such cellular mechanisms must provide a potent force for survival; otherwise, why would 98 percent of typhoid patients fail to become chronic carriers? 5) The continued study of infections, including the carrier state, with a view to understanding the abnormalities created by the multiplying intracellular microbe and the means by which the cell corrects these and eliminates the intruder, should open new vistas in chemotherapy and immunology.
Insights
Antibiotics effectively inhibit intracellular microbes, aiding in eradicating the typhoid carrier state. Further research is needed to understand microbial destruction mechanisms and cellular defense roles in infection clearance.
Area of Science:
- Microbiology
- Cell Biology
- Pharmacology
Background:
- Antibiotics rapidly penetrate mammalian cells, inhibiting microbial multiplication both intracellularly and extracellularly.
- Clinical observations align with laboratory findings regarding antibiotic efficacy against intracellular pathogens.
Purpose of the Study:
- To investigate the effectiveness of antibiotics in treating intracellular infections and the typhoid carrier state.
- To explore the mechanisms of microbial death within host cells and the role of cellular defense mechanisms.
Main Methods:
- Review of existing evidence on antibiotic penetration and activity within mammalian cells.
- Analysis of clinical data and laboratory observations related to intracellular infections and carrier states.
Main Results:
- Antibiotics are effective against intracellular microbes, comparable to extracellular activity.
- Prolonged antibiotic therapy (2-3 weeks) shows potential for eradicating the typhoid carrier state.
- Mechanisms of intracellular microbial death remain unclear, with hypotheses including antimicrobial substances and antibodies.
- Host cells possess natural defense mechanisms capable of clearing pathogens, potentially aided by antibiotics.
Conclusions:
- Antibiotic therapy, when properly selected and administered, can be a viable strategy for treating intracellular infections and carrier states.
- Understanding cellular defense mechanisms is crucial for developing novel chemotherapy and immunology approaches.
- Further research is warranted to elucidate the precise mechanisms of intracellular microbial destruction.
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