Ta. Ferguson et Jm. Herndon, THE IMMUNE-RESPONSE AND THE EYE - THE ACAID INDUCING SIGNAL IS DEPENDENT ON THE NATURE OF THE ANTIGEN, Investigative ophthalmology & visual science, 35(7), 1994, pp. 3085-3093
Purpose. To examine conditions that determine the nature of the blood-
borne, ACAID-inducing signal produced after intracameral injection of
antigen. Methods. Balb/c mice were splenectomized, rested, and injecte
d in the anterior chamber with various antigens. Two days later the an
imals were bled, the plasma and white cells were isolated, and these f
ractions were transferred to naive mice(with spleens). Recipients were
immunized subcutaneously within 2 to 7 days and delayed type hypersen
sitivity was assessed 10 to 14 days after immunization by challenge wi
th the appropriate antigen. Results. The antigens HSV-1, TNP-coupled c
ells, and P815 tumors cells induced a soluble ACAID-inducing signal fo
und in the plasma portion of blood. The soluble protein antigens bovin
e serum albumin (BSA) and conalbumin induced a cell-associated signal.
When T-cells were included with protein antigens, a soluble (not cell
ular) ACAID-inducing signal was induced. Conclusions. Particulate anti
gens, such as HSV-1 and P815, that elicit intraocular T-cell responses
or antigens that contain T-cells (e.g., TNP cells) induce a soluble,
ACAID-inducing signal. Soluble antigens (e.g., BSA and conalbumin) ind
uce a cell-associated ACAID signal. Additionally, T-cells are capable
of modulating the type of ACAID signal produced. These results show th
at two methods of delivering the ACAID signal exist that are dependent
on the nature of the antigen and the presence of T-cells. The authors
conclude that the eye shows great versatility in regulating potential
ly damaging immune responses.