Although RA has been extensively researched, its cause is still unclear. Studies
in families have shown that susceptibility to the disease is inherited. However, not every predisposed
individual actually develops RA. The causes of RA are still unclear, and our
genes may be only partly to blame. For example, people carrying the genetic variant known as human leukocyte
antigen (HLA) DR4 may be at increased risk of developing RA. This variation is manifested in white blood
cells and plays a role in helping the body distinguish between its own cells and non-self invaders. Molecular
biologists have managed to identify the amino acid sequences in the HLA molecule that are primarily
responsible for the associations seen in RA. |