Camelid immunoglobulins differ from all other known antibodies and contradi
ct all common theories on antibody diversity. It was demonstrated that up t
o 75% of all serum proteins are immunoglobulin G (IgG) molecules lacking li
ght chains. IgG(2) and IgG(3), which only consist of heavy chains, have a l
ow molecular weight which improves their biodistribution and allows a bette
r tissue penetration. Of special importance is the long complementary deter
mining region (CDR) loop which inserts deep into the active site of an enzy
me. This binding property was only observed in experiments to gain structur
al data and to point out the extraordinary value of heavy chain antibodies
as biochemical and pharmacological tools. The acquisition and absorption of
adequate amounts of colostral immunoglobulins are essential to the health
of the neonate, Pre-colostrum serum IgG levels in camelids are low, with co
ncentrations of 0.26 +/- 0.23 mg/ml. Maximum IgG levels are reached after 2
4 h and kept at a plateau with concentrations of 24.52 +/- 8.8 mg/dl. IgG c
oncentrations above 10 mg/ml. indicate a successful passive transfer. IgG l
evels decline after 2-5 weeks and a marked increase is observed between 1 a
nd 2 months, indicating that the immune system of the neonate has started t
o mature. A number of different tests are available for the assessment of I
gG serum levels. Single radial immunodiffusion (SRID) is the only method th
at specifically measures serum IgG concentrations. It is a reliable assay t
o test failure of passive transfer (FPT). FPT is a major factor in neonatal
mortality in camelids, but very little has been published so far. Therapeu
tic administration of colostrum will provide passive protection against inf
ectious diseases for a 2-3-week period of risk, and the intravenous adminis
tration of 20-40 ml of camelid plasma helps to combat FPT.