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Clinical Science
JAMA. 1964;187(6):442-447. doi: 10.1001/jama.1964.03060190058015

Infection With Artificially Propagated Eaton Agent (Mycoplasma pneumoniae)

Implications for Development of Attenuated Vaccine for Cold Agglutinin-Positive Pneumonia

  1. R. B. Couch, MD;
  2. T. R. Cate, MD;
  3. R. M. Chanock, MD
  1. Bethesda, Md
  2. From the National Institute of Allergy and Infectious Diseases, National Institutes of Health, Department of Health, Education, and Welfare.

Since this article does not have an abstract, we have provided the first 150 words of the full text.

Excerpt

IN RECENT YEARS there has been considerable progress in defining the etiology of atypical pneumonia. One of the important causes of this disease is the agent described by Eaton et al in 1944.1 This agent has been associated with cold agglutinin-positive atypical pneumonia in controlled epidemiologic investigations as well as in volunteer studies.2, 3 In addition, Eaton agent has been shown to cause febrile respiratory disease without pneumonia.4

Recently it has been shown that the Eaton agent is not a virus but a pleuropneumonia-like organism which can be cultivated on a cell-free artificial medium.5 The agent has been designated Mycoplasma pneumoniae.6

With the demonstration that this agent was a pleuropneumonia-like organism (Mycoplasma), it was of interest to determine if strains propagated on an agar medium could infect man. In order to test this possibility volunteers free of detectable antibody were inoculated with two strains of

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