Leprosy is a chronic infectious disease caused by Mycobacterium leprae, whi
ch was discovered by G.H.A. Hansen in 1873. M. leprae is an exceptional bac
terium because of its long generation time and no growth in artificial medi
a. Entire sequencing of the bacterial genome revealed numerous pseudogenes
(inactive reading frames with functional counterparts in M. tuberculosis) w
hich might be responsible for the very limited metabolic activity of M. lep
rae. The clinical demonstration of the disease is determined by the quality
of host immune response. Th1-type immune response helps to kill the bacter
ia, but hosts are encroached upon when Th2-type response Is predominant. Th
e bacteria have affinity to the peripheral nerves and are likely to cause n
europathy. AL leprae/laminin-alpha2 complexes bind to alpha/beta dystroglyc
an complexes expressed on the Schwann cell surface. WHO recommends a chemot
herapy protocol [multidrug therapy (MDT)] which effectively controls the di
sease and contributes to the global elimination program. Leprosy has been s
tigmatized throughout history, and recent topics regarding the disease in J
apan are also discussed.