R. Desjardins et al., IMMUNOACTIVATING POTENTIAL OF MULTILAMELLAR LIPOSOME VESICLES (MLV) IN MURINE POPLITEAL LYMPH-NODE (PLN) TEST, International journal of immunopharmacology, 17(5), 1995, pp. 367-374
Immunoactivating properties of subcutaneously injected small unilamell
ar vesicles (SUV) and multilamellar liposome vesicles (MLV) were studi
ed in relation to different transition temperatures (Tc) of phospholip
ids. Liposome-induced proliferative reaction in the popliteal lymph no
de (PLN) was quantified by subsequent cytometric assay. Early cell act
ivation during the onset of PLN reaction was monitored by immunophenot
yping of lymphocyte subsets stained with a panel of monoclonal antibod
ies (mAbs) and gating the subset-specific large/activated cells. Injec
tion of MLV liposomes containing distearoyl phosphatidylcholine (DSPC)
and dipalmityl phosphatidylcholine (DPPC), characterized by relativel
y high Tc, resulted in a marked PLN reaction, increased numbers of CD4
(+), CD8(+), Ig(+) subsets and increased proportions of large/activate
d EAM(+) (CD69(+)) and CD25(+) (IL-2 receptor(+)) cells. The reaction
was dose and time dependent. In contrast, injection of MLV liposomes c
ontaining lipids of low Tc, such as egg phosphatidylcholine (egg PC) a
nd dimyristoyl phosphatidylcholine (DMPC), did not show any immunoacti
vation. In addition, there was a highly reduced immunoactivating poten
tial of small-size SUV liposomes over large-sized MLV of identical pho
spholipid composition. Generally, both lipid composition and vesicle s
ize appeared to be essential for the immunoactivating potential of lip
osomes. The data suggest a possible correlation between the Tc of the
phospholipid and the immunoactivating potential of the large-sized MLV
liposomes.