MYCOPLASMAL INFECTIONS IN CFS/FMS/GWI
In a majority of FMS, CFS and GWI patients examined we   and others, principally Dr. Daryl See of the University of California College   of Medicine, Irvine, are finding   strong evidence for mycoplasrnal blood infections that   can explain much if not most of their chronic signs and symptoms. In our   studies on GWI we have found mycoplasmal infections   in about one-half of approximately 200 patients, and these patients were   found to have principally one pathogenic species,
M. fermentans.   Moreover, in over one-half of the 200 civilians with CFS, FMS or   arthritis that we have examined, we are finding a variety of pathogenic mycoplasma species in the leukocyte fraction of blood   samples. The test that we use to identify mycoplasmal   infections, polymerase chain reaction, is very sensitive and highly specific.   This test is a dramatic improvement on the relatively insensitive serum   antibody tests that are routinely used to assay for systemic mycoplasmal infections.( xvi, xvii)
MYCOPLASMA CRITERIA FOR CAUSING DISEASE
   Before systemic mycoplasmal infections can be   considered important in causing disease, certain criteria must be fulfilled:   (xviii)The incidence rate among        diseased patients must be higher than in those without disease. This has        been found. Moreover, in asymptomatic adults mycoplasmal        infections have been found in very low incidence. (xvi)
More of the mycoplasma must be recoverable from diseased        patients than from those without disease. This has been found. (xvi,        xvii)
An antibody response must be        found at higher frequency in diseased patients than in those without        disease. This has been found with
M fermentans,        but usually not until the disease has progressed. M. fermentans hides inside cells and does not elicits strong immune response until near death.        (xix, xx)
A clinical response must be        accompanied by elimination of the mycoplasma.        Follow up studies on recovered patients indicate that they reverted to mycoplasma-negative phenotypes.( xvi, xvii)
Clinical response is differential        depending on the type of antibiotics. Recovery is achieved only with        antibiotics that are effective against the pathogenic mycoplasmas. (xvi, xvii)
The mycoplasma        must cause a similar disease in animal models using monkeys. Injection        of
M. fermentans resulted in        development of fulminant disease that leads to        death.(xx)
The mycoplasma        must cause a similar disease when administered to human subjects. The mycoplasmas were not administered to volunteers        because of ethical considerations to investigate if they cause a similar        disease.
A specific anti-mycoplasma antibody reagent or immunization protects        against disease. To our knowledge this has not been done. Therefore, six        out of eight of the above criteria have been fulfilled, at least for
M.        fernentans, strongly suggesting that        certain mycoplasmas can cause human disease.        Baseman and Tully(xxi) have reviewed the        literature on the role of mycoplasmal        infections in human disease and have concluded that they are important        factors or cofactors in a variety of chronic illnesses.
The identification of mycoplasmal   infections in the leukocyte blood fractions of a rather large subset of GWI   CFS and FMS patients suggests that mycoplasmas, and possibly other chronic infections as well, may be   important sources of morbidity in these patients. Our results show a high   incidence of mycoplasmal infections in blood of   patients diagnosed with, CFS/FMS. Mycoplasmas are   not easily detected but can be identified by Nucleoprotein Gene Tracking(xxii) and forensic PCR. In previous studies using   the Nucleoprotein Gene Tracking detection method, we found mycoplasmal infections in 50% of GWI patients.

NEW TREATMENTS FOR FMS, CFS AND GWI

   If such infections are important in these disorders, then appropriate   treatment with antibiotics should, result in clinical improvement and even   recovery.(xxiii) We have proposed treatment   recommendations for mycoplasmal infections that are   similar to those used to treat Lyme disease, caused by other slow-growing   intracellular bacteria that are difficult to identify and treat. For mycoplasmal blood infections long-term antibiotic   therapy, usually multiple 6-week cycles of doxycycline   (200-,300 mg/d), ciprofloxacin (1,500 mg/d), azithromycin   (500 mg/d) and clarithromycin (800-1,000 mg/d)(xxii,xxiii) are required, possibly because of the   intracellular location of mycoplasmas like M
. fermentans and M. penetrans,   and the slow-growing nature of these microorganisms. Nutritional support is   also important, and vitamins (esp. B, C, E, CoQ10),   minerals (Zinc, Selenium, Chromium), immunoenhancers,   and replacement of gut flora (Lactobacillus acidophillus)   are important as well as moderate exercise and dry saunas to remove   contaminated chemicals.
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