Modulating activity of mistletoe lectins 1 and 2 on the lymphatic system in BALB/c-mice

被引:9
作者
Beuth, J [1 ]
Stoffel, B [1 ]
Samtleben, R [1 ]
Staak, O [1 ]
Ko, HL [1 ]
Pulverer, G [1 ]
Wagner, H [1 ]
机构
[1] UNIV MUNICH,INST PHARMACEUT BIOL,D-80333 MUNICH,GERMANY
关键词
mistletoe lectins; VAA-1; VAA-2; Viscum album; thymocyte proliferation; maturation; emigration; BALB/c-mice;
D O I
10.1016/S0944-7113(96)80054-7
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The galactoside-specific lectin (mistletoe lectin-l, VAA-1) and the N-acetylgalactosamine-specific lectin (mistletoe lectin-2, VAA-2) were purified from aqueous mistletoe extract and checked for their immunoactive potency. Regular subcutaneous administration of the optimal immunomodulating VAA-1/VAA-2 dosage (1 ng lectin/kg body weight) could be shown to modulate thymocyte proliferation, maturation, emigration and activation in BALB/c-mice. Thus, the increase in thymocyte counts was statistically significant after VAA-2 treatment. However, analogue VAA-2 applications significantly decreased thymocyte proliferation. Determinations of lymphatic subsets revealed considerable upregulation (after VAA-1 treatment) and significant downregulation (after VAA-2, treatment) of immature L 3 T 4(+)/Lyt-2(+) thymic cells. Counts of mature cells expressing helper/inducer (L 3 T 4(+)) or suppressor/cytotoxic (Lyt-2(+)) phenotypes did not present remarkable differences after VAA-1/VAA-2 administration. Counts of BALB/c-mouse peripheral blood cells revealed evident (statistically non-significant) increases of lymphocytes (PBL) and monocytes (PBM) after VAA-1 treatment, however, cell counts after VAA-2 administration were comparable ro non-treated control animals. The determination of activated PBL expressing interleukin IL-2 receptors proved that VAA-1 induced a potent immunostimulation, since these cells were significantly enhanced after VAA-1 administration but not after VAA-2 treatment.
引用
收藏
页码:269 / 273
页数:5
相关论文
共 22 条
[1]  
BEUTH J, 1993, ARZNEIMITTEL-FORSCH, V43-1, P166
[2]  
BEUTH J, 1992, CLIN INVESTIGATOR, V70, P658
[3]  
BEUTH J, 1991, In Vivo (Attiki), V5, P29
[4]  
Beuth J., 1993, In Vivo (Athens), V7, P407
[5]  
BEUTH J, 1993, MED KLIN, V88, P287
[6]  
BEUTH J, 1993, LECTINS GLYCOBIOLOGY, P396
[7]  
Beuth J., 1994, DTSCH Z ONKOL, V26, P1
[8]   PRECURSORS OF T-CELL GROWTH-FACTOR PRODUCING CELLS IN THE THYMUS - ONTOGENY, FREQUENCY, AND QUANTITATIVE RECOVERY IN A SUBPOPULATION OF PHENOTYPICALLY MATURE THYMOCYTES DEFINED BY MONOCLONAL ANTIBODY-GK-1.5 [J].
CEREDIG, R ;
DIALYNAS, DP ;
FITCH, FW ;
MACDONALD, HR .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 158 (05) :1654-1671
[9]   IDENTITY OF THE N-TERMINAL SEQUENCES OF THE 3 A-CHAINS OF MISTLETOE (VISCUM-ALBUM L) LECTINS - HOMOLOGY WITH RICIN-LIKE PLANT TOXINS AND SINGLE-CHAIN RIBOSOME-INHIBITING PROTEINS [J].
DIETRICH, JB ;
RIBEREAUGAYON, G ;
JUNG, ML ;
FRANZ, H ;
BECK, JP ;
ANTON, R .
ANTI-CANCER DRUGS, 1992, 3 (05) :507-511
[10]   ELECTROPHORETIC ANALYSIS OF MAJOR POLYPEPTIDES OF HUMAN ERYTHROCYTE MEMBRANE [J].
FAIRBANKS, G ;
STECK, TL ;
WALLACH, DFH .
BIOCHEMISTRY, 1971, 10 (13) :2606-+