Recent physiological and anatomical studies have demonstrated that a major
fraction of brain interstitial and cerebrospinal fluid drains into cervical
lymph nodes (CLN) in a number of experimental animals, To investigate the
role of CLN in brain tumour immunity, temporal profiles of MHC class II mol
ecule expression and T lymphocyte subsets in brain tumours, CLN and other l
ymphoid tissues were analysed by immunocytochemistry. A total of 64 Wistar
rats weighing 250 g were used. Two weeks after the transplantation of C6 gl
ioma cells (10(6) cells/l mu l) into a rat brain, expression of MHC class I
I molecules was induced in the brain and all systemic lymphoid tissues exam
ined. However, the subsequent appearance of CD4 or CD8 positive cells was s
trictly confined to CLN, and coincided with the infiltration of such cells
into the brain tumour 2 weeks after transplantation. In the group of animal
s in which cervical lymphadenectomy was followed by intracerebral transplan
tation of C6 glioma cells, infiltration of CD4 or CDS positive cells into t
he brain tumour was delayed until 3 weeks after the transplantation, and th
e production of such cells was by the spleen. These results suggest that CL
N act as regional lymph nodes in brain tumour immunity.