In vitro Evaluation of Biofield Treatment on Viral Load Against Human Immunodeficiency-1 and Cytomegalo Viruses
In vitro Evaluation of Biofield Treatment on Viral Load Against Human Immunodeficiency-1 and Cytomegalo Viruses
复制标题
生物场治疗对人类免疫缺陷-1 和巨细胞病毒病毒载量的体外评价
DOI:
10.11648/j.ajhr.20150306.14
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发表时间:
2015
期刊:
影响因子:
--
通讯作者:
S. Jana
中科院分区:
文献类型:
--
作者:
M. Trivedi;A. Branton;Dahryn Trivedi;G. Nayak;Sambhu Mondal;S. Jana
Viral load quantification is the amount of particular viral DNA or RNA in a blood samples. It is one of the surrogate biomarker of AIDS. High viral load indicates that the immune system is failed to fight against viruses. The aim of this study was to evaluate the impact of biofield treatment on HIV-1 and HCMV in terms of viral loads as surrogate marker. The viral load assay was performed on stored stock cultures of HIV infected human plasma samples before and after 7 days of biofield treatment using Roche COBAS® AMPLICOR analyzer. Viral load (HIV-1 RNA and HCMV DNAaemia) was considered as surrogate marker for assessment of the impact of Mr. Trivedi’s biofield treatment in HIV infected stored plasma samples. The viral load quantification of HIV-1 RNA in infected stored plasma samples was significantly reduced by 65% in biofield treated group as compared to control. Additionally, viral load of HCMV DNAaemia in infected stored plasma samples was also reduced by 80% in the biofield treated group as compared to control. Because, children are more prone to HCMV infection and adults are generally liable to suffer from HIV-1 infection. As the biofield treatment has reduced HCMV DNAaemia, it could be beneficial for HIV infected children populations. Altogether, data suggest that biofield treatment has significantly reduced the viral load quantification in HIV-1 and HCMV infected stored plasma samples and could be a suitable alternative treatment strategy for AIDS patients in near future.
DOI:
10.1016/s0022-3476(95)70357-8
发表时间:
1995
期刊:
The Journal of pediatrics
影响因子:
--
作者:
Palumbo,PE;Kwok,S;Waters,S;Wesley,Y;Lewis,D;McKinney,N;Bardeguez,A;Connor,EM;Oleske,JM
通讯作者:
Oleske,JM