ORAL-ADMINISTRATION OF A BACTERIAL IMMUNOMODULATOR ENHANCES MURINE INTESTINAL LAMINA PROPRIA AND PEYER PATCH LYMPHOCYTE TRAFFIC TO THE LUNG - POSSIBLE IMPLICATIONS FOR INFECTIOUS-DISEASE PROPHYLAXIS AND THERAPY

被引:27
作者
RUEDL, C [1 ]
ALBIN, B [1 ]
BOCK, G [1 ]
WICK, G [1 ]
WOLF, H [1 ]
机构
[1] SUNY BUFFALO, SCH MED & BIOMED SCI, DEPT MICROBIOL, BUFFALO, NY 14260 USA
关键词
IMMUNOMODULATION; LAMINA PROPRIA LYMPHOCYTES; LOCAL IMMUNITY; LYMPHOCYTE MIGRATION; ORAL IMMUNIZATION; PEYER PATCHES LYMPHOCYTES;
D O I
10.1093/intimm/5.1.29
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
LW50020, a bacterial immunomodulator, is a preparation consisting of seven bacteria, commonly causing respiratory disease. When given orally, LW50020 has been shown to enhance the host defense of the respiratory tract. Intestinal lamina propria lymphocytes (LPL), Peyer's patch lymphocytes (PPL), and splenocytes from BALB/c mice gavaged either with LW50020 or carrier alone were isolated, labeled with either H33342, a supravital nuclear fluorochrome, or Cr-51, and injected i.v. into untreated, age-matched BALB/c mice. Two hours later, spleen, liver, lung, kidneys, Peyer's patch, and mesenteric lymph nodes of the recipients were harvested and screened for the presence of labeled cells. LPL from mice gavaged with carrier only (controls) migrated preferentially to the lung, PPL equally well to the lung, and the spleen and splenocytes were found mostly in the spleen. LPL and PPL from LW50020-treated mice were found in significantly larger numbers in the lungs of recipients than LPL and PPL from control animals. Both labeling techniques gave roughly the same results. Sixty-five per cent of LPL in the lung were Thy-1.2+ and 20% B cells. These findings should contribute to the understanding of parameters necessary for the assessment of the mode of action and efficacy of immunomodulation and vaccination via the mucosa-associated lymphoid tissue.
引用
收藏
页码:29 / 36
页数:8
相关论文
共 30 条
[1]
INTERCELLULAR-ADHESION MOLECULE-1 (ICAM-1) HAS A CENTRAL ROLE IN CELL CELL CONTACT-MEDIATED IMMUNE-MECHANISMS [J].
BOYD, AW ;
WAWRYK, SO ;
BURNS, GF ;
FECONDO, JV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (09) :3095-3099
[2]
INTRACELLULAR FLUORESCENT LABELING OF CELLS FOR ANALYSIS OF LYMPHOCYTE MIGRATION [J].
BRENAN, M ;
PARISH, CR .
JOURNAL OF IMMUNOLOGICAL METHODS, 1984, 74 (01) :31-38
[3]
CHEN K, 1986, J VIROL, V60, P614
[4]
ANTIBODY-PRODUCING CELLS IN PERIPHERAL-BLOOD AND SALIVARY-GLANDS AFTER ORAL CHOLERA VACCINATION OF HUMANS [J].
CZERKINSKY, C ;
SVENNERHOLM, AM ;
QUIDING, M ;
JONSSON, R ;
HOLMGREN, J .
INFECTION AND IMMUNITY, 1991, 59 (03) :996-1001
[5]
PREPARATION AND PURIFICATION OF LYMPHOCYTES FROM THE EPITHELIUM AND LAMINA PROPRIA OF MURINE SMALL-INTESTINE [J].
DAVIES, MDJ ;
PARROTT, DMV .
GUT, 1981, 22 (06) :481-488
[6]
MECHANISMS AND REGULATION OF LYMPHOCYTE MIGRATION [J].
DUIJVESTIJN, A ;
HAMANN, A .
IMMUNOLOGY TODAY, 1989, 10 (01) :23-28
[7]
VCAM-1 ON ACTIVATED ENDOTHELIUM INTERACTS WITH THE LEUKOCYTE INTEGRIN VLA-4 AT A SITE DISTINCT FROM THE VLA-4 FIBRONECTIN BINDING-SITE [J].
ELICES, MJ ;
OSBORN, L ;
TAKADA, Y ;
CROUSE, C ;
LUHOWSKYJ, S ;
HEMLER, ME ;
LOBB, RR .
CELL, 1990, 60 (04) :577-584
[8]
SPECIFIC IMMUNE-RESPONSE IN THE HUMAN RESPIRATORY-TRACT FOLLOWING ORAL IMMUNIZATION WITH LIVE TYPHOID VACCINE [J].
FORREST, BD ;
LABROOY, JT ;
ROBINSON, P ;
DEARLOVE, CE ;
SHEARMAN, DJC .
INFECTION AND IMMUNITY, 1991, 59 (03) :1206-1209
[9]
FURHWIRTH M, 1993, UNPUB ENHANCEMENT LO
[10]
MOUSE GUT T-LYMPHOCYTE - NOVEL TYPE OF T-CELL NATURE, ORIGIN, AND TRAFFIC IN MICE IN NORMAL AND GRAFT VERSUS HOST CONDITIONS [J].
GUYGRAND, D ;
GRISCELLI, C ;
VASSALLI, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1978, 148 (06) :1661-1667