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Department of Microbiology and Immunology, University of Louisville School of Medicine, Health Sciences Center, Louisville, KY 40292
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Abstract |
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, IL-12, IL-4, or IL-10 and additional functional patterns are displayed depending on whether the cytokine is present alone or with other cytokines and whether the cytokines are added before or concomitantly with the activating stimulus (LPS). Sequential treatment of macrophages with multiple cytokines results in a progression through multiple functional phenotypes. This ability to adapt to changing cytokine environments has significant in vivo relevance, as evidenced by the demonstration that macrophage functional phenotypes established in vivo in aged or tumor-bearing mice can be altered by changing their microenvironment. A concept of functional adaptivity is proposed that has important implications for therapeutic targeting of macrophages in chronic diseases that result in the dominance of particular functional phenotypes of macrophages that play a significant role in disease pathology. |
Introduction |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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, thus establishing the classical two-signal paradigm of activation of macrophage inflammatory function. More recently, Stein et al. (7) reported that IL-4 treatment of macrophages induced a unique phenotype characterized by elevated expression of mannose receptor and a unique pattern of functions that were in sharp contrast to those induced by IFN- treatment of macrophages (4). Additional functional phenotypes subsequently were reported to be generated by treatment of macrophages with a variety of agents, including the type 2 cytokines IL-10 and TGF
(8, 9, 10, 11), Although there appeared to be distinctions between the functional phenotypes induced by IL-4, IL-10, and TGF (4, 10, 11), several researchers hypothesized that macrophages develop into two major functional subsets that display inflammatory vs anti-inflammatory patterns of function in association with Th1 vs Th2 driven responses, respectively (12, 13, 14).
Although macrophages that accumulate in chronic pathologies either display predominantly inflammatory/cytotoxic activities (15, 16, 17, 18) or display predominantly anti-inflammatory activities (11, 14, 18, 19), it is not clear that only two functional patterns exist. To the contrary, evidence is accumulating that suggests that macrophages may display several unique functional patterns (8, 9, 10, 20). More than one functional subset of macrophages participates in acute inflammatory responses, the early phase of which is dominated by inflammatory and/or cytotoxic activities and the terminal phase of which is dominated by anti-inflammatory/tissue regenerative activities (21, 22, 23). How this transition from macrophage inflammatory to anti-inflammatory activities is orchestrated is not known. If the development of functional subsets of macrophages is stable (e.g., involves differentiation), the transition of the innate response from inflammatory/cytotoxic activities to wound resolution would require removal, by apoptosis or emigration, of the inflammatory macrophage subset. Conversely, if the development of functional subsets of macrophages involves differential regulation of signaling cascades (reversible adaptation), the macrophages displaying inflammatory/cytotoxic activities could be induced to change their functional pattern to anti-inflammatory/tissue regenerative activities. To address these issues, we set out to determine (1) whether treatment with IFN-, IL-12 (type 1 cytokines), IL-4, or IL-10 (type 2 cytokines) would promote a pattern of functions that was unique for each cytokine rather than promoting qualitatively similar inflammatory vs anti-inflammatory patterns for the type 1 vs type 2 cytokines, respectively, (2) if the cytokine-treated macrophages could continue to adapt such that sequential changes in the cytokine environment would progressively alter the pattern of functional capabilities displayed by the macrophages upon activation, and (3) if the anti-inflammatory macrophage subsets generated during chronic pathologies such as cancer or advanced age could be redirected to an inflammatory phenotype.
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Materials and Methods |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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B6D2/J and C57BL/6J female mice were obtained from The Jackson Laboratory. CB6F1/nia female mice at 18–24 mo of age were obtained through the National Institute for Aging. All animal protocols received prior approval of the Institutional Animal Care and Use Committee, and all experiments were performed in accordance with relevant guidelines and regulations.
Generation and activation of bone marrow-derived macrophages (BMM
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Bone marrow cells were harvested from femur and tibias of 6–10-wk-old B6D2F1/J mice (The Jackson Laboratory). The cells were cultured in RPMI 1640 (HyClone) supplemented with 5% FBS (Atlanta Biologicals), recombinant mouse M-CSF (10 ng/ml; R&D Systems) and L929 conditioned medium (15%) in Nunclon surface (Nunc) cell culture plates. Non-adherent cells were collected after 24 h and were cultured for 7 days in the supplemented medium in Corning/Costar ultralow attachment polystyrene culture plates, changing the medium once on day 4. On day 7, the live cells were purified by centrifugation over Fico/Lite-LM (Atlanta Biologicals). The resulting cell population was >98% CD11b-positive. The cells were resuspended in RPMI 1640 with 5% FBS, dispensed to standard 24- or 48-well cell culture plates with the indicated cytokines before activation by 24 h culture with 0.1 µg/ml LPS (Escherichia coli 011B). For cytokine treatment, the cells were cultured 24 h with IFN- (20 U/ml), IL-12 (5 ng/ml), IL-4 (20 ng/ml), or IL-10 (20 ng/ml) (all from R&D Systems). For FcR ligation studies, the cells were treated with 1 µg anti-FcRII/III (hybridoma clone 2.4G2) for 30 min on ice, washed and cultured for 4 h before stimulation with LPS. For LPS tolerance, the cells were cultured with 20 ng/ml LPS, washed, and stimulated with 1 µg/ml LPS for 24 h.
Purification of peritoneal macrophages
Peritoneal cells were obtained by peritoneal lavage of untreated mice (resident cells) or of mice injected i.p. 4 days before with 2 ml of thioglycollate broth (elicited cells) (B-D). The macrophages were enriched using MS columns on MiniMACS Separator (Miltenyi Biotec) by depletion with anti-CD19 and anti-CD5 microbeads (Miltenyi Biotec) per the manufacturer’s instructions. The resulting cell populations were >95% CD5–, CD19–, and CD11b+. To maximize purity of macrophage populations in studies comparing young and aged mice or control and tumor-bearing mice, the populations enriched by negative selection were further purified by positive selection with anti-CD11b microbeads, resulting in populations that were >98% CD5–, CD19–, and CD11b+. Peritoneal macrophages were activated as described for BMM.
Antibodies, Western blot, and cytokine assays
Western blots were performed on lysates of activated BMM using Abs reactive with inducible NO synthase (iNOS),3 arginase, Cox-2 (BD Biosciences Transduction Laboratoriess) or actin (Sigma-Aldrich). The cells were lysed in lysis buffer (25 mM Tris-HCl, 1% Triton X-100, 1% deoxycolate, 350 mM NaCl, and 10 mM EDTA) with a protease inhibitor mixture (Calbiochem). Proteins were quantitated and equal amounts of protein were separated in Criterion pre-cast gels (10% Tris-HCl). Proteins were transferred to nitrocellulose membranes using a Trans-Blot SD SemiDry electrophoretic transfer cell (Bio-Rad). Antibody-bound proteins were detected using an ECL (Amersham Biosciences), and the membranes were exposed to Kodak Biomax XL x-ray film. IL-4, IL-6, TNF-
, IL-12p70, MCP1, IL-1 ELISA were performed on the culture supernatants using kits from BD Pharmingen and R&D Systems. Alternatively, cytokine production was quantitated by the cytometric bead array (CBA) for inflammatory cytokines (BD Pharmingen) per the manufacturer’s instructions using a FACSCalibur flow cytometer (BD Pharmingen).
Tumor-bearing mice
Lewis Lung Carcinoma (3LLC) was generously provided by Professor Gordon Ross (James Brown Cancer Center, University of Louisville). 3LLC cells (105) were injected subcutaneously into 6–10-wk-old C57/Bl6J mice (The Jackson Laboratory). Macrophages were harvested from the mice when the tumor mass approached 1 cm3 (14–16 days).
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Results |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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to display distinct functional patterns upon LPS stimulation
To determine whether treatment of macrophages with different type 1 (IFN-, IL-12) or type 2 (IL-4, IL-10) cytokines would promote macrophage production of inflammatory vs anti-inflammatory cytokines, BMM were cultured for 24 h in one of the cytokines, thoroughly washed, and stimulated with LPS for 18–24 h. Analysis of the culture supernatant by ELISA revealed that both IL-4 and IFN- treatment enhanced the production of the inflammatory cytokines TNF- and IL-12 and inhibited the production of IL-10 (Fig. 1). However, these two patterns were distinct in that IFN- inhibited MCP-1 production whereas IL-4 enhanced MCP-1 production. IL-10 treatment resulted in a more anti-inflammatory phenotype insofar as IL-12 production was profoundly inhibited whereas IL-10 production was enhanced. This increase in IL-10 was not due to "carry-over" of rIL-10 as evidenced by the absence of detectable IL-10 in supernatant fluid from macrophage cultures treated with IL-10 but not activated by LPS (data not shown). To focus on, and more easily visualize, the patterns of LPS-induced cytokine production resulting from treatment of BMM with type 1 or type 2 cytokines, the cytokine response was normalized to that obtained by LPS stimulation of BMM without cytokine treatment. Using this format to view which cytokines were enhanced, unaffected, or reduced by a particular treatment protocol, it becomes apparent that treatment of BMM with IFN-, IL-12, IL-4, and IL-10 each induced a unique functional phenotype (Fig. 2) FcR ligation (24) and low dose LPS pretreatment (25, 26, 27) have been reported to result in unique patterns of cytokine production upon subsequent stimulation with LPS. To determine whether these patterns of cytokine production were similar to those promoted by the four cytokines presented above, the pattern of LPS-induced cytokine production was determined after treatment of BMM with either anti-FcRII/III or a low dose (20 ng/ml) of LPS. The response pattern to LPS stimulation resulting after FcR ligation, characterized by reduced TNF- and IL-12 production and enhanced IL-1 and IL-10 production, and the response pattern to LPS stimulation resulting after LPS pretreatment, characterized by reduced TNF-, IL-12, and IL-6 production and elevated IL-1, MCP-1, and IL-10 production, were uniquely distinct from each other and from each of the patterns promoted by the four cytokines reported above (Figs. 1 and 2). Overall, this panel of six ligands biased the macrophages to display one of six different response patterns upon subsequent stimulation with LPS. It should be noted that different macrophage populations (peritoneal vs bone marrow) do not respond identically to LPS (21) and that the same macrophage population from different strains of mice have been reported not to respond identically to LPS (9). Thus, the emphasis here is that six different treatments of B6D2F1/J BMM yielded six different patterns of response to LPS.
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-treated BMM enhanced iNOS and COX-2 expression without inducing detectable arginase expression (Fig. 3). However, LPS stimulation of IL-4-treated BMM enhanced iNOS and COX-2 and also induced arginase expression (Fig. 3), thus establishing that all three enzymes could be simultaneously expressed upon treatment with LPS and a type 2 cytokine. Treatment of BMM with IL-10 in combination with IL-4-abrogated LPS induction of both iNOS and COX-2 but further amplified expression of arginase (Fig. 3). The impact of IL-4 on BMM function thus was influenced by the presence of other cytokines during the treatment period.
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were stimulated with LPS either in the presence of or after a 24-h culture with IFN-, IL-4, or IL-10. The impact of IL-4 and IL-10, and to a lesser degree IFN-, was dramatically different when the cytokine was added concomitantly with the activating stimulus rather than 24 h before the activating stimulus (Fig. 4). Treatment with IL-4 before LPS stimulation enhanced production of all cytokines except IL-1 and IL-10, which it inhibited. In contrast, costimulation with IL-4 and LPS inhibited production of all cytokines except MCP-1 and IL-10, which it enhanced (Fig. 4). Treatment with IL-10 before LPS inhibited IL-12 and MCP-1 but only moderately inhibited or had no effect on production of the remaining cytokines. In contrast, when present during LPS stimulation, IL-10 profoundly inhibited production of all cytokines tested.
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To determine whether the pattern of functional capabilities established by treatment with a cytokine displayed stability indicative of an established subset of macrophages, BMM were treated for 24 h with IFN-, IL-10, or IL-4, washed free of the cytokine, and cultured for 24 h with an alternate cytokine before washing and stimulation with LPS. IFN--treated BMM subsequently cultured in IL-10 before LPS stimulation displayed a pattern of cytokine production clearly distinct from BMM stimulated with LPS directly after IFN- treatment (Fig. 5). Treating IFN--primed M with IL-10 resulted in a dramatic decrease in IL-12 and TNF- production and an equally dramatic increase in IL-10 production. Similar results were obtained when IL-10-treated M were cultured with IFN- before LPS stimulation or IL-4-treated M were cultured with IFN- before LPS stimulation (Fig. 5). In each case, changing the cytokine environment altered the functional pattern established by the first cytokine treatment. In some instances, the functional pattern observed after sequential cytokine treatment was similar, though not identical, to that obtained by treatment only with the second cytokine, as observed with IFN-
IL-10 group. In other instances, the functional pattern observed after sequential cytokine treatment was unique, distinct from that observed after treatment with either cytokine alone, as observed with IL-4IFN- treatment (Fig. 5). The transient nature of the effect of cytokine treatment was also revealed by delaying addition of LPS for 24 h after removal of the cytokine. Such an exposure of the M to an in vitro environment "free" of exogenous cytokine muted the functional changes that were observed upon activation immediately following cytokine treatment, as observed the most dramatically in the IL-10-treated group (Fig. 5).
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that have been considered to be relatively immature. This raised the possibility that the observed ability to adapt to changing environments was a trait of a relatively immature macrophage population and would not be observed in mature macrophage populations. To determine whether a similar multistep sequential shift in functional phenotype could be induced in mature macrophages treated ex vivo, thioglycollate-elicited peritoneal macrophages were purified and activated with LPS either immediately ex vivo or after a sequential 24-h culture with IFN- (Fig. 6a), IFN- followed by IL-10 (Fig. 6b), IFN- followed by IL-10 followed by IL-4 (Fig. 6c), or IFN- followed by IL-10 followed by IL-12 (Fig. 6d). The macrophages were washed after each cytokine treatment. Compared with peritoneal macrophages activated with LPS without cytokine treatment, treatment with IFN- enhanced production of IL-12, TNF-, and IFN- while reducing production of MCP-1 and IL-10 (Fig. 6a). Subsequent treatment with IL-10 altered this response, tempering production of IL-12, TNF- and IFN- and restoring production of MCP-1 and IL-10 (Fig. 6b). Treatment with IL-4 following the sequential treatment with IFN- and IL-10 induced a third sequential shift in functional phenotype, yielding a pattern of cytokine production that was distinct from the first two patterns (Fig. 6c). Production of IL-12, TNF-, IFN-, and IL-6 were elevated and production of IL-10 was reduced. Treatment with IL-12 after sequential treatment with IFN- and IL-10 resulted in a fourth pattern of cytokine production that bore some similarities to the pattern originally imprinted by IFN- treatment (Fig. 6d). In summary, peritoneal macrophages, like BMM, changed their functional phenotype multiple times in response to changes in the cytokine environment.
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The above studies addressed the stability of macrophage functional phenotypes generated by 24-h cytokine treatment. To examine the functional adaptivity of macrophages whose phenotype had been established in vivo for a prolonged period of time, we investigated two pathological states known to dramatically alter macrophage function: cancer and immunosenescence. Animals bearing metastatic tumors have been reported to develop a unique subset of macrophages that accumulate in the tumor mass as well as in distal sites such as the spleen and peritoneal cavity and that suppress inflammatory and immune responses (14, 30, 31). To determine whether these suppressive macrophages represented a stable subset of macrophages, resident peritoneal cells were removed from mice bearing a s.c. 3LL tumor and the macrophages purified by magnetic bead selection. Compared with resident peritoneal cells from normal mice, the macrophages from tumor-bearing mice displayed reduced production of TNF-, IFN-, and IL-6 and enhanced production of MCP-1 and IL-10 upon LPS stimulation (Fig. 7a). Treatment of the macrophages for 24 h with IFN- before stimulation with LPS resulted in a shift in the pattern of cytokine production that was similar in M from both normal and tumor-bearing mice (Fig. 7b). Production of TNF- and IFN- was increased and production of MCP-1 and IL-10 was decreased by the IFN- treatment.
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, IFN-, IL-12, and MCP-1 compared with macrophages from young mice (Fig. 7c). Treatment of the macrophages from aged mice for 24 h with IFN- before LPS stimulation in vitro enhanced production of TNF- and IL-12 and reduced production of IFN- and MCP-1. The IFN--treated macrophages from aged and young mice displayed nearly identical patterns of cytokine production (Fig. 7d), indicating that both populations of macrophages retained the ability to adapt to a different cytokine environment. |
Discussion |
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TopAbstractIntroductionMaterials and MethodsResultsDiscussionDisclosuresReferences |
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and IL-12 production, iNOS and COX-2 expression) and inhibited anti-inflammatory activity (IL-10 production). The number of potential synergizing and antagonizing agonists in a tissue microenvironment is huge and would include cytokines, chemokines, hormones (including steroid hormones, catecholamines, insulin), TLR ligands, and a wide variety of other ligands (e.g., leptin, histamine, Ig, complement, cell adhesion molecules, peroxisome proliferator-activated receptor ligands, apoptotic cells, etc.) (1, 8, 21, 33, 34, 35, 36, 37). All of these have been reported to modify the functional response pattern of macrophages to an activating stimulus such as LPS. The number of functions macrophages potentially can express is also large. Gene array studies indicate that an activating signal such as LPS can induce expression of hundreds of genes in macrophages and that the expression of these genes is differentially regulated by different cytokines (9, 10, 20). Given the number of genes expressed by macrophages, the number of modulating and activating ligands, and the synergistic/antagonistic relationship of those ligands, it is apparent that macrophages may be capable of displaying a very large array of diverse functional phenotypes.
Since Stein et al. (7) reported that treatment of macrophages with IL-4 induced a functional phenotype distinct from that induced by treatment with IFN-, several investigators have reported that treatment of macrophages with different cytokines can differentially alter their functional potential (8, 10, 11). However, none of these studies has addressed whether these macrophages, once functionally polarized, retain the ability to continue to adapt to changes in their environment by progressively changing their functional phenotype. This is an important issue. The reversibility of macrophage functional phenotype would have significant therapeutic value in chronic diseases such as cancer, autoimmune inflammatory disease, or infection with mycobacteria, schistosomes, or toxoplasma, which result in the dominance of particular functional phenotypes of macrophages that play a significant role in disease pathogenesis (11, 14, 15, 16, 17, 18, 19). The current data indicate that the functional phenotype of these macrophages can be changed and that macrophages may progress from one functional phenotype to another as the microenvironmental influences change. Therefore, as an alternative to the concept of stable macrophage subsets, we propose a model of functional adaptivity as a basis for understanding macrophage function in physiologically dynamic responses. The model of functional adaptivity predicts not only that macrophages adapt to microenvironmental signals via differential regulation of function, but also that macrophages can progressively change their functional phenotype in response to progressive changes in the environmental signals.
The concept of functional adaptivity provides an alternative perspective on macrophage biology and macrophage function in inflammation and disease. For example, the inflammatory response involves dramatic changes in tissue environment, changes which progress through proinflammatory, destructive, anti-inflammatory and reparative stages. Whether inflammatory macrophages apoptose or emigrate from the site of inflammation when the inflammatory signals subside (38) is still debated. An alternative, though not necessarily exclusive, possibility is that, in response to the changing environment of the successfully debrided wound, the functional phenotype of the macrophages changes to allow participation in wound resolution. Thus the TGF-producing anti-inflammatory macrophages in remitting lesions of animal models of multiple sclerosis may have been derived from the TNF-/NO-producing inflammatory macrophages that populated the active lesions during acute disease (39, 40). There are several reports of macrophages or macrophage-derived cells changing their functional phenotype in response to environmental changes. Microglia are monocyte-derived sessile cells in the CNS that display neuroprotective activities such as production of TGF and brain-derived neurotrophic factor (41, 42, 43). However, inflammatory episodes in the brain cause the microglia to become highly motile "macrophage-like" cells displaying proinflammatory and neurotoxic activities (41, 42, 43). Myeloid dendritic cells have been reported to revert to macrophage characteristics (44, 45, 46) or, under the influence of Trance, to display the functional and phenotypic characteristics of multinucleated osteoclasts (47). Thus it appears that tissue macrophages and macrophage-derived cells retain their ability to adapt to changes in their environment by altering the pattern of functions they express.
In chronic disease states, where tumors continuously produce immunomodulatory cytokines (30, 31) or a subset of T cells are chronically activated (11, 17, 19), macrophages displaying a particular functional phenotype may predominate. As shown herein, their function can be changed by providing them with a proinflammatory environment. Thus, manipulation of the cytokine environment in situ should convert them into inflammatory and/or cytotoxic effectors (30). Indeed, cytokine therapies targeting NK cells and T cells do have a significant impact on proinflammatory and cytotoxic activities of tumor-associated macrophages (see Ref. 48 and S. Watkins, N. Egilmez, and R. Stout, manuscript in preparation). Macrophages in aged animals display reduced inflammatory and cytotoxic activity (32). Since this age-related functional phenotype can be changed by placing them in a proinflammatory environment, the age-related functional phenotype may be a result of macrophage adaptation to age-related changes in the tissue environment rather than to inherent defects in the macrophages. Thus the age-related inflammatory deficiencies of macrophages may be responsive at least transiently to cytokine therapy (21).
A critical point of this study is that the functionally polarized macrophages which accumulate in a wide variety of pathologies retain their functional adaptivity and thus their functional phenotype can be changed given the appropriate stimulus. In the context of controlling macrophage-mediated pathologies, current therapeutic approaches are designed to inhibit the biological activity of cytokines and metabolites produced by the macrophages in chronic pathological conditions (15, 49, 50, 51). Based on the results of the present study, therapeutic approaches could be targeted toward changing the functional phenotype of the macrophages, i.e., changing the pattern of cytokines, metabolites, and enzymes produced by the macrophages.
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Acknowledgments |
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Disclosures |
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Footnotes |
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1 This research was supported by grants from the National Institute for Aging (AG20972; to R.D.S.), the Kentucky Lung Cancer Research Fund (to R.D.S.), the National Institute of Allergy and Infectious Disease (AI48850; to J.S.), the National Multiple Sclerosis Society (RG3374; to J.S.), the Arthritis Foundation (to J.S.), and by the Commonwealth of Kentucky Research Challenge Trust Fund (to R.D.S. and J.S.). 
2 Address correspondence and reprint requests to Dr. Robert D. Stout, Department of Microbiology and Immunology, 319 Abraham Flexner Way, Health Sciences Center, University of Louisville School of Medicine, Louisville, KY 40292. E-mail address: bobstout{at}louisville.edu
3 Abbreviations used in this paper: iNOS, inducible NO synthase; M, macrophage; BMM, bone marrow-derived macrophages; CBA, cytokine bead array.
Received for publication February 2, 2005. Accepted for publication April 29, 2005.
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 L. Arnold, A. Henry, F. Poron, Y. Baba-Amer, N. van Rooijen, A. Plonquet, R. K. Gherardi, and B. Chazaud Inflammatory monocytes recruited after skeletal muscle injury switch into antiinflammatory macrophages to support myogenesis J. Exp. Med., May 14, 2007; 204(5): 1057 - 1069. [Abstract] [Full Text] [PDF]
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L. K. Weaver, P. A. Pioli, K. Wardwell, S. N. Vogel, and P. M. Guyre Up-regulation of human monocyte CD163 upon activation of cell-surface Toll-like receptors J. Leukoc. Biol., March 1, 2007; 81(3): 663 - 671. [Abstract] [Full Text] [PDF]
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S. K. Watkins, N. K. Egilmez, J. Suttles, and R. D. Stout IL-12 Rapidly Alters the Functional Profile of Tumor-Associated and Tumor-Infiltrating Macrophages In Vitro and In Vivo J. Immunol., February 1, 2007; 178(3): 1357 - 1362. [Abstract] [Full Text] [PDF]
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J. P. Edwards, X. Zhang, K. A. Frauwirth, and D. M. Mosser Biochemical and functional characterization of three activated macrophage populations J. Leukoc. Biol., December 1, 2006; 80(6): 1298 - 1307. [Abstract] [Full Text] [PDF]
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 S. Kumar and R. Jack Invited review: Origin of monocytes and their differentiation to macrophages and dendritic cells Innate Immunity, October 1, 2006; 12(5): 278 - 284. [Abstract] [PDF]
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 J. Pestka and H.-R. Zhou Toll-Like Receptor Priming Sensitizes Macrophages to Proinflammatory Cytokine Gene Induction by Deoxynivalenol and Other Toxicants Toxicol. Sci., August 1, 2006; 92(2): 445 - 455. [Abstract] [Full Text] [PDF]
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Yimin and M. Kohanawa A Regulatory Effect of the Balance between TNF-{alpha} and IL-6 in the Granulomatous and Inflammatory Response to Rhodococcus aurantiacus Infection in Mice J. Immunol., July 1, 2006; 177(1): 642 - 650. [Abstract] [Full Text] [PDF]
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