In vivo migration of labeled autologous natural killer cells to liver metastases in patients with colon carcinoma
© Matera et al; licensee BioMed Central Ltd. 2006
Received: 18 April 2006
Accepted: 14 November 2006
Published: 14 November 2006
Besides being the effectors of native anti-tumor cytotoxicity, NK cells participate in T-lymphocyte responses by promoting the maturation of dendritic cells (DC). Adherent NK (A-NK) cells constitute a subset of IL-2-stimulated NK cells which show increased expression of integrins and the ability to adhere to solid surface and to migrate, infiltrate, and destroy cancer. A critical issue in therapy of metastatic disease is the optimization of NK cell migration to tumor tissues and their persistence therein. This study compares localization to liver metastases of autologous A-NK cells administered via the systemic (intravenous, i.v.) versus locoregional (intraarterial, i.a.) routes.
Patients and methods
A-NK cells expanded ex-vivo with IL-2 and labeled with 111In-oxine were injected i.a. in the liver of three colon carcinoma patients. After 30 days, each patient had a new preparation of 111In-A-NK cells injected i.v. Migration of these cells to various organs was evaluated by SPET and their differential localization to normal and neoplastic liver was demonstrated after i.v. injection of 99mTc-phytate.
A-NK cells expressed a donor-dependent CD56+CD16+CD3- (NK) or CD56+CD16+CD3+ (NKT) phenotype. When injected i.v., these cells localized to the lung before being visible in the spleen and liver. By contrast, localization of i.a. injected A-NK cells was virtually confined to the spleen and liver. Binding of A-NK cells to liver neoplastic tissues was observed only after i.a. injections.
This unique study design demonstrates that A-NK cells adoptively transferred to the liver via the intraarterial route have preferential access and substantial accumulation to the tumor site.
Effector functions mediated by cells of the immune system are thought to play a crucial role in the control of tumor development and progression. However, it has been difficult to distinguish the part played by individual immune cell subsets in these processes. T cells that mediate tumor-specific responses are generally considered to be the major anti-tumor effectors. However, cells responsible for mediating innate or natural immunity have been recently recognized to also contribute to anti-tumor defense. Extensive investigation of tumor growth and metastasis in animal models suggests that NK cells are early participants in the immune response and are particularly effective in eliminating blood-borne metastases [1, 2]. In contrast, T cells are the effector cells responsible for specific, long-lasting immunity.
In addition to their direct anti-tumor functions [3–7], NK cells can mobilize adaptive immune response  presumably by promoting the maturation of dendritic cells (DC) [9–14] and by providing them with antigenic material derived from tumor cell lysis [15, 16]. DC mediate both protective and autoimmune responses, depending on their maturational state and soluble factors present in the tissue microenvironment [17, 18]. In the liver, for example, Kupffer cells and LSEC constitutively express the anti-inflammatory cytokines, IL-10 and transforming growth factor beta (TGF-β), while hepatocytes secrete IL-10 in response to autocrine and paracrine TGF-β. These cytokines could inhibit maturation of liver DC [19, 20]. Therefore, delivery of NK cells to the liver milieu could shift the balance from tolerogenic to immunogenic conditions. The hypothesis we are entertaining is that NK cell-mediated DC maturation in the liver could alter the suppressive local environment, enhance immune responses, and lead to the elimination of tumor cells metastasizing to the liver.
The efficacy of adoptive immunotherapy of solid tumors depends on the localization of therapeutic cells to tissues. This in turn is influenced by the route of administration and access of the cells to tumor. Liver metastases are solely fed by the hepatic artery, and injection of chemotherapeutic agents  and immune cells  via this route has proven to be effective in controlling the spread of tumors of the digestive tract, whose initial metastasis site is the liver.
The success of adoptive immunotherapy is also critically dependent on the migratory properties of the effector cells and their ability to access tumor cells in situ. High expression levels of molecules belonging to the integrin and to the human-leukocyte-function-associated antigen families, namely LFA-1 and very late antigen (VLA)-4, which interact with adhesion molecules on the tumor endothelium, is a characteristic feature of activated NK cells . NK cells have the ability to migrate to, infiltrate and kill cancer cells in solid tumor tissues [24, 25] and eliminate established tumors and metastases. Based on their selective ability to rapidly (1–5 h) respond to 22 nM IL-2 by a temporal adherence to solid surface, we have previously defined subpopulations of NK cells, namely activated A-NK cells, which constitute 4–30% of fresh peripheral blood NK cells and are notably different from the non-adherent IL-2 activated cells (NA-NK). A-NK cells produce significant levels of the DC-maturating cytokines IFN-γ, IL1-β and TNF-α and display potent anti-tumor activities in vivo and in vitro .
Injection of A-NK cells into the hepatic artery may be an ideal approach to treating tumors metastasizing to the liver. Although this approach to therapy has been previously used, no formal evidence exists for the superior tumor infiltrating capacity of intraarterially (i.a.)-delivered versus intravenously (i.v.)-delivered A-NK cells. Here we compare in the same patient the efficiency of tumor localization of ex vivo generated clinical grade A-NK cells delivered via locoregional i.a. versus i.v. injections.
Patients, materials and methods
Protocol design and patient's characteristics
Site of metastasis
A-NK cell generation
Cells were generated for therapy under conditions conforming to current good manufacturing practice (GMP), i.e., using animal-free serum components and reagents approved for human therapy and accompanied by certificates of analysis (COA). PBMC were isolated from venous blood by Ficoll-Hypaque (Lymphoprep, 1.077 g/ml; Nycomed Pharma, Oslo, Norway) gradient centrifugation and washed in RPMI 1640 (Gibco cat. No. 61870-028) containing 1% (v/v) defibrinated autologous plasma (DAP). The PBMC were suspended at the concentration of 1 × 107 cells/ml in RPMI 1640 containing 10% DAP, 100 U/ml penicillin, 2 mM L-glutamine, 3 mg/ml sodium bicarbonate, Pen/strep (100 U/ml) (culture medium) and 5 mM phenylalanine methyl ester (PME) at 7.0–7.2 pH. Following a 30 min incubation at RT to deplete monocytes, cells were extensively washed in medium, counted and suspended in the adherence medium supplemented with 1 mM CaCl2, 1 mM MgCl2, 100 U/ml heparin and 6,000 IU/ml of rIL-2 (Chiron s.r.l., Siena, Italy), obtained from the local Molinette's Hospital Pharmacy and designated for human use. After 3 h at 37°C in a 5% CO2 atmosphere non-adherent cells were removed by washing (x3) with pre-warmed medium, and adherent cells (A-NK cell precursors) were counted in four sample flasks with a grid bottom and multiplied for the total number of culture flasks. A feeder layer consisting of rIL-2 (50 IU/ml)-stimulated monocyte-depleted PBMC irradiated at 5,000 rads suspended in culture medium containing 1 × 106/ml of Con A (10 μg/ml) and 6,000 IU/ml rIL-2 was added to each flask. Cells were incubated for 15 days and were fed every four days with rIL-2 (6,000 IU/ml) culture medium to adjust cell density to 1.5 × 106/ml.
A-NK cell labeling and administration
A-NK cells were harvested, washed, counted and their phenotype was determined. An aliquot was sent for sterility analysis. The remaining cells were suspended in 20 ml clinical grade 0.93% NaCl solution containing 25% DAP, 6,000 IU/ml rIL-2 and 37 MBq 111In-oxine (Altana Pharma, Milan, Italy). A-NK cells were generated twice for each patient and the same number of cells was labeled on both occasions. After 15 min at room temperature cells were washed twice in 0.93% NaCl saline containing 25% DAP and 6,000 IU/ml rIL-2. The cell pellet was then suspended in 10 ml 0.93% NaCl containing 20% human albumin (clinical grade) and cells were injected i.a. After 30 days, A-NK cells were again administered, this time i.v. Paracetamol(Acetaminophen) (Perfalgan, UPSA Lab, Braine-l'Alleud, Belgium) (1 g) and 1 × 107 rIL-2 were given s.c. 30 h before and 48 h after these injections. Each patient was injected with the same number of labeled cells, generated in separate cultures at each of the two time points.
Evaluation of labeling efficiency
Labeling efficiency was defined as the ratio between free and cell-bound tracer, evaluated in a gamma counter as the cpm of radioactivity contained in the washing supernatant and in the cell pellet.
A-NK cell migration evaluation
Planar whole-body and single-photon emission-computed tomography (SPET) acquisitions were performed by two-head gamma camera (VARICAM-ESCINT, General Electric, Milwankee, WI, USA) equipped with "medium energy" collimators for 111In, with 20% window and energy peaks at 173 and 247 KeV. Planar whole-body acquisitions were performed at 1,6,24,72 and 96 h and SPET acquisitions at 6 and 96 h.
Localization of A-NK cells to liver metastases
To estimate the extent of the non-pathological liver parenchyma, patients were given an i.v. injection of 99mTc Phytate (FITATEC) (AMERSHAM SORIN, Saluggia, Italy) before A-NK cell administration. Liver images were acquired after 10 min by the gamma camera equipped with "low energy" collimator with 20% window and energy peak at 140 KeV. 111In labeled A-NK images were acquired by the gamma camera equipped with "medium energy" collimators, as described above.
Phenotypic analysis of A-NK cells
A-NK cells were analyzed by flow cytometry on day fifteen. One million cells were incubated for 20 min at 4°C with mouse anti-human simultest CD3FITC/CD16.CD56PE or with γ1 FITC/γ2a PE isotype controls (Becton Dickinson, San Jose, CA, USA). Flow cytometric analysis was performed using a FACScan flow cytometer CellQuest (v2.1q) software (Becton Dickinson).
Growth and phenotypic characteristics of A-NK cells
Biological characteristics of injected A-NK
Final A-LAK recovery3
1.2 × 108
8 × 107
6 × 106
5 × 108
5 × 108
2.8 × 108
1.5 × 108
5 × 106
1.2 × 109
5 × 108
1.2 × 108
8 × 107
3.2 × 106
1.6 × 109
5 × 108
2.5 × 108
9 × 107
3.6 × 106
6 × 108
5 × 108
1.3 × 108
5 × 107
1 × 106
6 × 108
5 × 108
1.3 × 108
8 × 107
5 × 106
2.3 × 109
5 × 108
NA-NK cell labeling efficiency and stability
The mean efficiency of labeling was 56% (range 42–67%) (Table 2).
Migration of A-NK cells to the liver
Localization of A-NK cells to tumor nodules
As the first metastatic site of gastric and colon cancer, the liver is a critical check point for systemic disease progression. The liver is rich in immune cells, including DC precursors, NK cells and T lymphocytes. Generation of CD8+ tumor-specific T cells, which mediate anti-tumor responses in the liver, is enhanced by activated NK cells, which facilitate maturation of DC [8–14]. However, a suppressive liver environment hampers functional maturation of DC and the consequent activation of the adaptive immune response. Therapy with activated NK cells can therefore be envisaged as a means to breaking liver tolerance and to boosting antigen-specific anti-tumor responses. The efficiency of adoptive cellular immunotherapy of cancer strongly depends on the type, number and the route of delivery of effector cells that are expected to reach malignant tissues after their transfer.
We demonstrate that ex vivo expanded A-NK cells efficiently home to liver metastases and only accumulate therein, when they gain direct access to the portal system. This route may favor the localization and concentration of immune effector cells in the tumor, since liver metastases are fed with arterial blood. However, preferential localization in the tumor is also likely to depend on the intrinsic homing characteristics of the injected cells. NK cells have a regulated expression of a number of integrins that may play a role in their localization. In situ immunohistochemical staining has shown NK-cell localization to the red pulp of the spleen and the sinusoid regions of the liver. Few NK cells are present in other solid organs and, surprisingly, there are relatively few NK cells in lymph nodes . NK cells present in the liver sinusoids are strategically located to detect and kill arriving metastatic cancer cells, and their accumulation at this site is favored by chemokine ligands present in the LSEC . The LSEC cytokine environment, with IL-2 produced by resident T cells  and IL-15 and IL-12 produced by Kupffer cells , might be expected to potentiate homing and cytotoxic functions of NK cells. Indeed, genes involved in NK-cell homing, cytotoxicity and cytokine secretory functions are overexpressed in hepatic NK cells compared to blood NK cells , but their expression profile is similar to that of IL-2-activated blood NK cells. It is, therefore, very likely that the radioactivity detected in the metastatic areas of the liver is due to interactions between labeled A-NK cells and the tumor LSEC.
The ability of A-NK cells to penetrate the tumor tissue is relevant to their potential use as carriers of anti-tumor drugs and as direct killers of tumor cells. In experimental in vivo tumor models, NK cells are more frequently found to localize tumors which are also sensitive to NK cell killing in vitro . Besides direct anti-tumor activities of NK cells, their localization in the liver tumor area would be important for the maturation of DCs, possibly through the production of IFN-γ and other cytokines.
Two A-NK subsets predominated in our three patients after a fifteen-day expansion: CD16+CD56+CD3+ in patient #1 and CD16+CD56+CD3- in patients #2 and #3. Adhesion to tissue cells expressing the relevant receptors is the main property of these cells, and it is conferred, among other molecules, by N-CAM, which is present on NK cells and a subpopulation of NKT cells [31, 32]. NKT cells are the population best represented in the liver . In our study, preferential 111In labeling of these A-NK subpopulations (both NK and NKT cells) in the metastatic compared to normal liver was observed.
We found a prompt localization of A-NK cells to the lung after i.v. injection, as also shown by other in vivo studies [24, 25, 35]. Transit of NK cells to the lung via the peripheral blood circulation is likely to play a surveillance role in vivo, since radiolabeled tumor cells injected i.v. are eradicated by NK cells before they enter the lung . Radioactivity detected in our study is most probably attributable to cell-bound rather than to cell-free tracer for two reasons. First, the absence of excretion of radioactivity over the observation period (ref  and our data not shown) indicates extended survival of injected A-NK cells. Second, free tracer would not have been taken up by the tumor and was not taken up after i.v. administration (Fig. 5B bottom). The half-life of adoptively transferred NK cells is about 7–10 days . This is particularly true in the permissive environment of liver sinusoids.
We have performed an imaging study of the biodistribution of ex vivo activated, adoptively-transferred autologous A-NK cells and demonstrated their differential localization in normal hepatic parenchyma and liver metastases. The unique opportunity offered by this study of comparing different administration routes in the same patient, allowed unambiguous demonstration that A-NK cells localize to liver metastases only when injected locoregionally. This finding has important implications for the design of future immunotherapy protocols based on the principle that autologous A-NK cells adoptively transferred to the liver via the arterial route have preferential access and substantial accumulation to the tumor site.
adherent Natural Killer
liver sinusoidal endothelial cells
phenylalanine methyil ester
counts per minute
single-photon emission-computed tomography.
We are in debt with the Blood Bank of the Molinette Hospital for expert collaboration. The work was supported by MIUR, Regione Piemonte (Oncology project) and the CERMS/COES project funded by the "Compagnia di San Paolo/FIRMS". Informed consent was obtained from all patients.
- Cooper MA, Fehniger TA, Caligiuri MA: The biology of human natural killer-cell subsets. Trends Immunol. 1991, 22: 633-640. 10.1016/S1471-4906(01)02060-9.View ArticleGoogle Scholar
- Soloski MJ: Recognition of tumor cells by the innate immune system. Curr Opin Immunol. 2001, 13: 154-162. 10.1016/S0952-7915(00)00198-9.View ArticlePubMedGoogle Scholar
- Kuppen PJ, Gorter A, Hagenaars M, Jonges LE, Giezeman-Smits KM, Nagelkerke JF, Fleuren G, van de Velde CJH: Role of NK cells in adoptive immunotherapy of metastatic colorectal cancer in a syngeneic rat model. Immunol Rev. 2001, 184: 236-243. 10.1034/j.1600-065x.2001.1840121.x.View ArticlePubMedGoogle Scholar
- Dillman RO, Duma CM, Schiltz PM, DePriest C, Ellis RA, Okamoto K, Beutel LD, de Leon C, Chico S: Intracavitary placement of autologous lymphokine-activated killer (LAK) cells after resection of recurrent glioblastoma. J Immunother. 2004, 27: 398-404. 10.1097/00002371-200409000-00009.View ArticlePubMedGoogle Scholar
- Ishikawa E, Tsuboi K, Saijo K, Harada H, Takano S, Nose T, Ohno T: Autologous natural killer cell therapy for human recurrent malignant glioma. Anticancer Res. 2004, 24: 1861-1871.PubMedGoogle Scholar
- Klingemann HG, Martinson J: Ex vivo expansion of natural killer cells for clinical applications. Cytotherapy. 2004, 6: 15-22. 10.1080/14653240310004548.View ArticlePubMedGoogle Scholar
- Palumbo JS, Talmage KE, Massari JV, La Jeunesse CM, Flick MJ, Kombrinck KW, Jirousková M, Degen JL: Platelets and fibrinogen increase metastatic potential by impeding natural killer-mediated elimination of tumor cells. Blood. 2005, 105: 178-185. 10.1182/blood-2004-06-2272.View ArticlePubMedGoogle Scholar
- Fan Z, Yu P, Wang Y, Wang Y, Fu ML, Liu W, Sun Y, Fu YX: NK cell activation by LIGHT triggers tumor specific CD8+ T cell immunity to reject established tumors. Blood. 2005; Oct. 13,
- Gerosa F, Baldani-Guerra B, Nisii C, Marchesini V, Carra G, Trinchieri G: Reciprocal activating interaction between natural killer cells and dendritic cells. J Exp Med. 2002, 195: 327-333. 10.1084/jem.20010938.PubMed CentralView ArticlePubMedGoogle Scholar
- Moretta A: Natural killer cells and dendritic cells: rendezvous in abused tissues. Nat Rev Immunol. 2002, 2: 957-964. 10.1038/nri956.View ArticlePubMedGoogle Scholar
- Piccioli D, Sbrana S, Melandri E, Valiante NM: Contact-dependent stimulation and inhibition of dendritic cells by natural killer cells. J Exp Med. 2002, 195: 335-341. 10.1084/jem.20010934.PubMed CentralView ArticlePubMedGoogle Scholar
- Cooper MA, Fehniger TA, Fuchs A, Colonna M, Caligiuri MA: NK cells and DC interaction. Trends Immunol. 2004, 25: 47-52. 10.1016/j.it.2003.10.012.View ArticlePubMedGoogle Scholar
- Fujii S, Liu K, Smith C, Bonito AJ, Steinman RM: The linkage of innate to adaptive immunity via maturing dendritic cells in vivo requires CD40 ligation in addition to antigen presentation and CD80/86 costimulation. J Exp Med. 2004, 199: 1607-1618. 10.1084/jem.20040317.PubMed CentralView ArticlePubMedGoogle Scholar
- Pan PY, Gu P, Li Q, Xu D, Weber K, Chen SH: Regulation of dendritic cell function by NK cells: mechanisms underlying the synergism in the combination therapy of IL-12 and 4-1BB activation. J Immunol. 2004, 172: 4779-4789.View ArticlePubMedGoogle Scholar
- Galetto A, Buttiglieri S, Forno S, Moro F, Mussa A, Matera L: Drug- and cell-mediated antitumor cytotoxicities modulate cross-presentation of tumor antigens by myeloid dendritic cells. Anticancer Drugs. 2003, 14: 833-843. 10.1097/00001813-200311000-00010.View ArticlePubMedGoogle Scholar
- Mocikat R, Braumuller H, Gumy A, Egeter O, Ziegler H, Reusch U, Bubeck A, Louis J, Mailhammer R, Riethmüller G, Koszinowski U, Röcken M: Natural killer cells activated by MHC class Ilow targets prime dendritic cells to induce protective CD8 T cell responses. Immunity. 2003, 19: 561-569. 10.1016/S1074-7613(03)00264-4.View ArticlePubMedGoogle Scholar
- Dhodapkar MV, Steinman RM, Krasovskya J, Munza C, Bhardwaja N: Antigen-specific inhibition of effector T cell function in humans after injection of immature dendritic cells. J Exp Med. 2001, 193: 233-238. 10.1084/jem.193.2.233.PubMed CentralView ArticlePubMedGoogle Scholar
- Schuler-Thurner B, Schultz ES, Berger TG, Weinlich G, Ebner S, Woerl P, Bender A, Feuerstein B, Fritsch PO, Romani N, Schuler G: Rapid induction of tumor-specific type I T helper cells in metastatic melanoma patients by vaccination with mature, cryopreserved, peptide-loaded monocyte-derived dendritic cells. J Exp Med. 2002, 195: 1279-1288. 10.1084/jem.20012100.PubMed CentralView ArticlePubMedGoogle Scholar
- Lau AH, Thomson AW: Dendritic cells and immune regulation in the liver. Gut. 2003, 52: 307-314. 10.1136/gut.52.2.307.PubMed CentralView ArticlePubMedGoogle Scholar
- Pillarisetty VG, Shah AB, Miller G, Bleier JI, DeMatteo RP: Liver dendritic cells are less immunogenic than spleen dendritic cells because of differences in subtype composition. J Immunol. 2004, 172: 1009-1117.View ArticlePubMedGoogle Scholar
- Zanon C, Grosso M, Clara R, Alabiso O, Chiappino I, Miraglia S, Martinetti R, Bortolini M, Rizzo M, Gazzera C: Combined regional and systemic chemotherapy by a mini-invasive approach for the treatment of colorectal liver metastases. Am J Clin Oncol. 2001, 24: 354-359. 10.1097/00000421-200108000-00007.View ArticlePubMedGoogle Scholar
- Kobari M, Egawa S, Shibuya K, Sunamura M, Saitoh K, Matsuno S: Effect of intraportal adoptive immunotherapy on liver metastases after resection of pancreatic cancer. Br J Sur. 2000, 87: 43-48. 10.1046/j.1365-2168.2000.01336.x.View ArticleGoogle Scholar
- Allavena P, Bianchi G, Paganin C, Giardina G, Mantovani A: Regulation of adhesion and transendothelial migration of natural killer cells. Nat Immunol. 1996, 15: 107-116.Google Scholar
- Brand JM, Meller B, Von Hof K, Luhm J, Bahre M, Kirchner H, Frohn C: Kinetics and organ distribution of allogeneic natural killer lymphocytes transfused into patients suffering from renal cell carcinoma. Stem Cells Dev. 2004, 13: 307-314. 10.1089/154732804323099235.View ArticlePubMedGoogle Scholar
- Morris MA, Ley K: Trafficking of natural killer cells. Curr Mol Med. 2004, 4: 431-438. 10.2174/1566524043360609.View ArticlePubMedGoogle Scholar
- Vujanovic NL, Yasumura S, Hirabayashi H, Lin WC, Watkins S, Herberman RB, Whiteside TL: Antitumor activity of subsets of human IL-2-activated natural killer cells in solid tissues. J Immunol. 1995, 154: 281-289.PubMedGoogle Scholar
- Yokoyama WM, Kim S, French AR: The dynamic life of natural killer cells. Ann Rev Immunol. 2004, 22: 405-429. 10.1146/annurev.immunol.22.012703.104711.View ArticleGoogle Scholar
- Vermijlen D, Seynaeve C, Luo D, Kruhoffer M, Eizirik DL, Orntoft TF, Wisse E: High-density oligonucleotide array analysis reveals extensive differences between freshly isolated blood and hepatic natural killer cells. Eur J Immunol. 2004, 34: 2529-2540. 10.1002/eji.200324712.View ArticlePubMedGoogle Scholar
- Doherty DG, O'Farrelly C: Innate and adaptive lymphoid cells in the human liver. Immunol Rev. 2000, 174: 5-20. 10.1034/j.1600-0528.2002.017416.x.View ArticlePubMedGoogle Scholar
- Li Z, Lin H, Yang S, Diehl AM: Murine leptin deficiency alters Kupffer cell production of cytokines that regulate the innate immune system. Gatroenterology. 2002, 123: 1304-1310. 10.1053/gast.2002.35997.View ArticleGoogle Scholar
- Nagler A, Lanier LL, Phillips J: Constitutive expression of high-affinity interleukin 2 receptors on human CD16-negative natural killer cells in vivo. J Exp Med. 1990, 171: 1527-1533. 10.1084/jem.171.5.1527.View ArticlePubMedGoogle Scholar
- Li S, Xu J, Makarenkova VP, Tjandrawan T, Vakkila J, Reichert T, Gooding W, Lagenaur CF, Achim CL, Chambers WH, Herberman RB, Whiteside TL, Vujanovic NL: A novel epitope of N-CAM defines precursors of human adherent NK cells. J Leukoc Biol. 2004, 76: 1187-1199. 10.1189/jlb.0802386.View ArticlePubMedGoogle Scholar
- Seino K, Taniguchi M: Functional roles of NKT cell in the immune system. Front Biosci. 2004, 9: 577-587.View ArticleGoogle Scholar
- Franitza S, Grabovsky V, Wald O, Weiss I, Beider K, Dagan M, Darash-Yahana M, Nagler A, Brocke S, Galun E, Alon R, Peled A: Differential usage of VLA-4 and CXCR4 by CD3+CD56+ NKT cells and CD56+CD16+ NK cells regulates their interaction with endothelial cells. Eur J Immunol. 2004, 34: 1333-1341. 10.1002/eji.200324718.View ArticlePubMedGoogle Scholar
- Kjaergaard J, Hokland ME, Agger R, Skovbo A, Nannmark U, Basse PH: Biodistribution and tumor localization of lymphokine-activated killer T cells following different routes of administration into tumor-bearing animals. Cancer Immunol Immunother. 2000, 48: 550-560. 10.1007/PL00006673.View ArticlePubMedGoogle Scholar
- Prlic M, Blazar BR, Farrar MA, Jameson SC: In vivo survival and homeostatic proliferation of natural killer cells. J Exp Med. 2003, 197: 967-976. 10.1084/jem.20021847.PubMed CentralView ArticlePubMedGoogle Scholar
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