Very little is currently known about HTLV-3 and HTLV-4. It is unclear how many people may be infected with these viruses, whether they can spread from person to person and become established within a community, or even if they cause illness.
However, given the fact that a related virus, HTLV-1 is known to cause serious diseases, it is important to monitor the possible spread of these viruses and to determine their disease potential. There is also still much to be learned about HTLV-1 and at this time there is no cure or treatment.
The appearance of these new viruses serves as a reminder that increased contact between humans and primates enhances the likelihood that a virus will cross species, as occurred when HIV was transmitted from chimpanzees into humans. Our experience with HIV has taught us that we need to be vigilant when new viruses arise in humans.
A key protein of HTLV-1 that is necessary for the virus to cause disease goes by the name of Tax-1. This protein regulates the expression of other viral genes and has the ability to transform normal cells into cancerous ones and produce tumors in experimental animals.
Dr. Susan Marriott’s laboratory studied the molecular interactions of the Tax-1 protein for many years to understand how it functions in causing cancer. Her laboratory also investigated the Tax protein of HTLV-3, termed Tax-3. Tax-3 is quite similar to Tax-1 in its genetic sequence, and it may share its molecular properties. They found that Tax-3 has a similar distribution within cells and has a similar ability to interact with important regulatory proteins in cells as does Tax-1. Furthermore, Tax-3 contains a region called a PDZ domain that is critical for the ability of Tax-1 to cause cells to become cancerous, suggesting that Tax-3 may also be capable of transforming cells.
In addition, Dr. Marriott worked with collaborators at the CDC to develop reagents that can be used to determine the prevalence of HTLV-3 infection in humans and to investigate the possibility that this virus infection is associated with a human disease.