INFECTIOUS HEPATITIS – HAV & HEV CAUSES A BENIGN AND SELF LIMITED DISEASE. COINFECTION BY HDV & HBV RARELY DEVELOPS CHRONIC HEPATITIS. ACUTE COINFECTION BY HDV & HBV VARY IN MILD TO FULMINANAT HEPATITIS. WHEREAS, PERSISTENT INFECTION AND CHRONIC HEPATITIS ARE THE HALLMARKS OF HBV & HCV VIRUSES. INSTANCES OF SEVERE AND RAPIDLY PROGRESSIVE CHRONIC HBV & HCV HEPATITIS ARE BEING RECOGNIZED WITH INCREASING FREQUENCY IN PATIENTS WITH  HIV INFECTION.

WHERE HBV IS DNA - VIRUS, THE HCV & HIV ARE RNA –VIRUSES. IN HBV   INFECTION IMMUNOLOGICALLY MEDIATED HEPATOCYTES NECROSIS BY SENSITIZED CYTOTOXIC T-CELLS, ATTRIBUTE TO CELLULAR EXPRESSION OF VIRAL ANTIGENS. WITH INTERANCE OF HBV-DNA INTO THE HOST GENOME VIRAL REPLICATION CEASES, INFECTIVITY ENDS AND ACTIVE LIVER DAMAGE SUBSIDES. THE PATHOGENESIS OF THE HCV & HIV INFECTIONS IS ALSO IMMUNOLOGICALLY MEDIATED LIVER DAMAGE. HOWEVER, HIV IS CHARACTERIZED BY PROFOUND SUPPRESSION OF T-CELL MEDIATED IMMUNITY. WHEREIN, IN ADDITION TO T –CELL DEPLETION THERE ARE ALSO QUALITATIVE DEFECTS IN T – CELL FUNCTION WITH A SELECTIVE LOSS OF T – CELL MEMORY. B- CELL IMMUNE ACTIVATION IN HIV – PATIENTS IS UNABLE TO MOUNT APPRECIABLE ANTIBOBY RESPONSES TO NEW ANTIGENS, LEADING TO GREATER SEVERITY OF THE VIRAL HEPATITIS. FATAL CONDITION IS SUPPORTED BY OPPORTUNISTIC INFECTIONS, SECONDARY NEOPLASMS, NEUROLOGIC AND METABOLIC DISORDERS. CLINICO – SYMPTOMATIC AND PATHOMECHANIC MEDICAL TREATMENTS ENSURE LITTLE HELP, AND DEATH IS SURE.

ALL ATTEMPTS ARE MADE TO PROVIDE AUTOPATHY TREATMENTS TO PATIENTS BEFORE THE ‘FULL BLOWN’ HBV / HCV – HIV STAGE OF THE DISEASE HAS REACHED. REGIROUS ‘TREATMENT – ASSISTS’ IS CONTINUED. AAA – THERAPY IS STARTED AS EARLY AS POSSIBLE. BLOOD TRANSFUSION AND INTERFERON THERAPY IS AVOIDED. HYDROCORTISONE [EFFCORLIN], ANTIBIOTICS [ROXITHROMYCIN], ANTIOXIDANT [FREE CAD] CALCIUM GLUCONATE WITH VIT-C & B-12 [CALCIUM SANDOZ] INJECTIONS, WATER-MINERALS-GLUCOSE SUBSTITUTIONS AND VITAMIN-K INJECTIONS ARE ADDED. GRADUALLY, THE ‘TREATMENT – ASSISTS’ IS DISCONTINUED. WITHIN THREE TO SIX MONTHS AFTER AAA - THERAPY ALONG WITH ABOVE NOTED MEDICAMENTOSIS PATIENTS SHOW DRASTIC IMPROVEMENT. ANTIOXIDANT [ BD ], CALCIUM SANDOZ INJECTIONS [ I / M , WEEKLY ] PERITOL / PERICORT [ OD ] AND ANY SYMPTOMATIC TREATMENT [ IF NEEDED ] ARE CONTINUED. WITHIN NINE TO ELEVEN MONTHS AFTER THE FIRST COURSE, THE SECOND COURSE OF AAA – THERAPY IS REINSTITUTED. PATIENTS ARE ADVISED TO CONTINUE TAKING HOT WATER – LEMON DRINKS, THREE – FOUR TIMES A DAY, TULSI [INDIAN TERMINOLOGY] – FATT FREE CURD, AND BOILED ‘ APPLE – GLUCOSE ‘ AS MAJOR PORTION OF THE DAILY MEAL.

MINIMUM AT THREE MONTHS INTERVALS MASTER CHECK-UP [PARAMEDICAL INVESTIGATIONS] AND SPECIFIC AUTOPATHY TESTS ARE CERTAINLY CONDUCTED. MAJORITY [> 75%] OF THE PATIENTS RECOVERS. VERY FEW PATIENTS NEED THIRD COURSE OF THE AAA – AUTOPATHY TREATMENT. RELAPSE OF THE HEPATITIS OF HIV / HBV – HCV HAS NOT YET BEEN SEEN.