e had need to take any other oral medicine for other conditions he was advised to take such other medicine at least two hours before the AntivirtÒ or two hours after. He was also advised to sleep under insecticide-treated mosquito bed-net (to prevent malaria) and to run the HIV/AIDS status tests (CD4 counts, viral loads, HIV-antibody and HIV-antigen) every month and submit the results. When he became negative for both HIV-antibody and HIV-antigen, he was asked to stop the treatment but continue testing his blood for HIV-antibody, every month.
After being on the MSAMS-treatment for 20 months the patient became HIV-negative (both antibody and antigen) while his CD4 count improved from 685 to 820. Following cessation of the treatment, he has continued to test negative to HIV-antibody for 10 consecutive months and he has not been complaining of symptoms of HIV/AIDS. Results of his HIV/AIDS status tests are as on Table 1.
Immune deficiency is defined by deficit of blood lymphocytes  . It is not a clinical abnormality. Some animals or human-beings can have low blood lymphocytes-counts from birth (genetic defect) but when a person or an animal that
Table 1. Results of HIV/AIDS-status tests of a patient, following treatment with medicinal synthetic aluminum-magnesium silicate.
ND = Not done.
was born with normal blood lymphocytes-counts develops significantly low lymphocytes-counts the disease is termed acquired immune deficiency syndrome (AIDS).
AMS-Nanoparticles displace HIV from its hosts’ cells, by electrostatic bonding of their surfaces to positive charges on the virus. Thus the first stage in the viral replication is inhibited  . They also bond to negative charges on HIV-infected cells, with their positively charged edges and destroy them by the same mechanism with which AMS disintegrates drug-capsules  . Thus “hidden” HIV-infections are unmasked. As Nanoparticles, they have access to all HIV-infected cells in all organs/tissues including the “sanctuary cells”.
Reason existing ARVs do not achieve permanent cure of HIV/AIDS could be that their molecules are too large to cross physiological barriers. For that limitation, they do not reach HIV infections “hidden” in some cells. So, even when viral loads in blood of patients whom they are used to treat become undetectable, the infection remains “hidden”. When such patients stop taking ARVs the hidden infections multiply and viremia reoccurs. For that reason, HIV/AIDS is said to be incurable.
Since the MSAMS (Antivirt®) is made of Nanoparticles, it crosses physiological barriers and reaches HIV and HIV-infected cells in every organ/tissue. And since it acts by a physical effect (mopping electrically charged pathogens), it is safe for prolonged treatment. So, it is only a matter of time for HIV-infection, in each treated patient, to get terminated.
In an earlier clinical trial  of the MSAMS, CD4 counts of HIV-positive patients (663.60 ± 45.43) increased (P = 0.00) to 1461.78 ± 339.84 within 10 months but in this patient, even after 20 months on the treatment, his CD4 increased to only 820. That failure of CD4 counts to rise very high delayed asking the patient to go for cure-confirmatory tests even when his clinical state suggested he had recovered. Some individuals have genetic defects in blood lymphocytes-counts. This patient may be one of such people.
That a HIV/AIDS patient with CD4 count of only 820 tested HIV-negative for both antibody and antigen suggests that our insistence that people on the MSAMS’ clinical trial must have ≥1500 CD4 before they can be considered for HIV-status tests may not be right in every case.
Longest window period for HIV is only six months. So, for a person who was HIV-positive to remain HIV-negative for 10 months without being on any ARV confirms our earlier observation that-treatment with the MSAMS terminates HIV infections  . If the patient does not get exposed again, he may remain HIV-negative for life.
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