TREATING PATIENTS BASED ON IMMUNE SUBTYPES

Abstract

This document provides methods and materials for treating patients following an assessment of immune subtypes such as an assessment of peripheral blood phenotypes. For example, methods and materials for treating a mammal having a medical condition after assessing a mammal's level of CD14.sup.+/DR.sup. cells (e.g., CD14.sup.+/DR.sup. monocytes) and level of CD4.sup.+ cells (e.g., CD4.sup.+ T cells) and classifying the mammal has being likely to experience a favorable or unfavorable medical outcome based at least in part on the mammal's level of CD14.sup.+/DR.sup. cells and level of CD4.sup.+ cells are provided.

Claims

1. (canceled)

2. A method for treating cancer, wherein said method comprises administering, to a mammal identified as having cancer and an elevated level of CD14.sup.+/DR.sup. cells, (i) a chemotherapy with or without surgery and (ii) an anti-CTLA-4 antibody, Ipilumimab, or an anti-PD1 antibody.

3. The method of claim 2, wherein said mammal is a human.

4. The method of claim 2, wherein said cancer is glioblastoma or lymphoma.

Description

DESCRIPTION OF THE DRAWINGS

[0018] FIG. 1A is a survival curve for glioblastoma patients having (a) normal levels of CD14.sup.+/DR.sup. cells and CD4.sup.+ cells, (b) a normal (low) level CD14.sup.+/DR.sup. cells and a reduced level of CD4.sup.+ cells, or (c) an elevated level of CD14.sup.+/DR.sup. cells and a reduced level of CD4.sup.+ cells. FIG. 1B is a survival curve for glioblastoma patients when plotted based on the CD4.sup.+ levels alone. FIG. 1C is a survival curve for glioblastoma comparing patients with either CD4.sup.+ or CD14.sup.+/DR.sup. levels at abnormal levels compared to patients with normal values of both.

[0019] FIG. 2 is a graph plotting the level of CD4.sup.+ cells (cells/L) versus the level of CD14.sup.+/DR.sup. cells (percent of CD14.sup.+ cells that are DR.sup.) for sepsis patients. For sepsis patients, the cut off values were 63% DR.sup. and 650 CD4.sup.+ cells/L.

[0020] FIG. 3 is a graph plotting percent survival versus days for sepsis with patients grouped on peripheral immunity. Patients were grouped based on normal or elevated levels of CD14.sup.+/DR.sup. cells and normal or reduced levels of CD4.sup.+ cells.

[0021] FIG. 4 is a graph plotting the level of CD4.sup.+ cells (cells/L) versus the level of CD14.sup.+/DR.sup. cells (percent of CD14.sup.+ cells that are DR.sup.) for lymphoma patients.

[0022] FIG. 5 is a graph plotting overall survival (percent) versus time (days) for lymphoma patients categorized by their peripheral blood phenotype. Patients were grouped according to normal or increased percent of CD14.sup.+/DR.sup. cells and reduced or normal levels of CD4.sup.+ cells. The normal (DR (<10%) and normal CD4 (>500 cells/L)) and the normal DR and low CD4 groups overlap on the survival curve.

[0023] FIG. 6 is a graph plotting the overall survival (percent) versus time (days). The black line represents patients whose monocytes had normal HLA-DR expression (n=11; CD14.sup.+HLA-DR.sup.low/neg<10% of CD14.sup.+ monocytes). The gray line represents patients whose monocytes had a loss of HLA-DR expression (n=29; CD14.sup.+HLA-DR.sup.low/neg monocytes; monocytes where >10% of CD14.sup.+ monocytes had lost HLA-DR expression.

[0024] FIG. 7 contains graphs plotting the levels of CD14.sup.+HLA-DR.sup.lo/neg monocytes in chronic lymphocytic leukemia (CLL). Blood from 29 CLL patients and 15 healthy volunteers were used for immune phenotyping. There was no age difference (median of 58 vs. 59 years, respectively; p=0.2896). Patients were eligible for the clinical trial (ClinicalTrials.gov NCT00562328) if diagnosed with previously untreated high risk CLL using standard criteria and did not meet guidelines for conventional treatment. Blood was collected before initiation of treatment and 6, 9, and 12 months after completion of treatment in patients who had a sustained response. The percent of CD14.sup.+ cells with a loss of HLA-DR staining was determined and compared between CLL patients and healthy volunteers (HV; upper left). CLL patients with a sustained response to treatment had a decrease in the frequency of HLA.sup.DR.sup.log/negCD14.sup.+ monocytes 12 months after completion of treatment (diamonds) compared to measurement prior to treatment (upper right). Kaplan-Meyer survival curve comparing CLL patients with elevated ratios (>2.5 standard deviations) of CD14.sup.+HLA-DR.sup.log/neg monocytes when compared to healthy volunteers (dashed line) or with ratios similar to those seen in healthy volunteers (solid line; bottom panel).

[0025] FIGS. 8A-8B demonstrate the relationship of the presence of peripheral blood CD14.sup.+HLA-DR.sup.lo/neg monocytes and intratumoral accumulation of CD14.sup.+ cells in renal cell carcinoma. FIG. 8A is a Kaplan-Meier curve of the survival of 375 patients with renal cell carcinoma based on the classification of hi, medium, lo, and no intratumoral staining. FIG. 8B is a graph plotting the correlation of intratumoral CD14 staining and the amount of peripheral blood CD14.sup.HLA-DR.sup.lo/neg monocytes from the same patients.

[0026] FIG. 9 is a graph plotting flow cytometry and Q-PCR data for HLA-DR expression. Blood samples from healthy volunteers and cancer patients were stained for CD14 and HLA-DR. RNA was isolated from CD14.sup.+ populations from the same individuals. Quantitative RT-PCR was performed to determine the level of expression by assessing the crossing point (Cp) of each PCR reaction. The percentage of CD14.sup.+HLA-DR.sup.log/neg monocytes were then plotted against the Cp of each PCR reaction.

DETAILED DESCRIPTION

[0027] This document provides methods and materials for treating patients following an assessment of immune subtypes such as an assessment of peripheral blood phenotypes. For example, this document provides methods and materials for treating a mammal having a medical condition after assessing a mammal's level of CD14.sup.+/DR.sup. cells (e.g., CD14.sup.+/DR.sup. monocytes) and level of CD4.sup.+ cells (e.g., CD4.sup.+ T cells) and classifying the mammal has being likely to experience a favorable or unfavorable medical outcome based at least in part on the mammal's level of CD14.sup.+/DR.sup. cells and level of CD4.sup.+ cells.

[0028] As described herein, an appropriate treatment option for a particular medical condition (e.g., cancer, sepsis, autoimmunity, or trauma) can be selected following an assessment of the level of CD14.sup.+/DR.sup. cells within a mammal. Such an assessment can include, for example, determining the level of CD14.sup.+/DR.sup. cells within a mammal and comparing the determined values to values of CD14.sup.+/DR.sup. cells for that particular condition or to values from healthy volunteers to assess whether the level is an altered level (e.g., an increased level of CD14.sup./DR.sup. cells or a complete or substantially complete loss of all CD14.sup.+/DR.sup. cells). It is noted that healthy volunteers can have an average of about 6% DR.sup.. In cases of immune suppression, this percentage can be higher. In cases of autoimmunity, it can go very low (e.g., virtually all can be DR.sup.+).

[0029] In addition, the level of CD4.sup.+ cells within the mammal can be determined and compared to cut-off values of CD4.sup.+ cells for that particular condition or compared to healthy volunteers to assess whether the level is a normal level, an elevated level (e.g., high level of CD4.sup.+ cells), or a reduced level (e.g., low level of CD4.sup.+ cells). In some cases, a single CD14.sup.+/DR.sup. cell cut-off value can be used to assess whether the level of CD14.sup.+/DR.sup. cells is an elevated level (e.g., a high level of CD14.sup./DR.sup. cells) or a reduced level (e.g., a low level of CD14.sup.+/DR.sup. cells) and/or a single CD4.sup. cell cut-off value can be used to assess whether the level of CD4.sup.+ cells is a normal level (e.g., a typical level of CD4.sup.+ cells) or a reduced level (e.g., a low level of CD4.sup.+ cells). Within particular diseases, the levels for either the CD14.sup.+/DR.sup. or CD4.sup.+ cells can be considered as high or extremely high. Once the level of CD14.sup.+/DR.sup. cells and/or the level of CD4.sup.+ cells is determined for a mammal having a particular medical condition, the mammal's likelihood of experiencing either a favorable or unfavorable medical outcome for that particular medical condition can be determined based, at least in part, on the normal, elevated, or reduced level of CD14.sup./DR.sup. cells by itself or in some cases by the addition of the categorization (e.g., normal, elevated, or reduced level) of CD4.sup. cells.

[0030] The level of CD14.sup.+/DR.sup. cells and/or the level of CD4.sup.+ cells can be determined using a sample (e.g., a blood sample) obtained from the mammal to be assessed. Once obtained, the sample can be treated such that the level of CD14.sup.+/DR.sup. cells and the level of CD4.sup.+ cells present can be determined. Cell staining and immunofluorescence techniques (e.g., flow cytometry) can be used to determine the level of CD14.sup.+/DR.sup. cells and/or the level of CD4.sup.+ cells. For example, anti-CD14, anti-HLA-DR, and anti-CD4 antibodies can be used to perform flow cytometry in order to determine the level of CD14.sup.+/DR.sup. cells and the level of CD4.sup.+ cells present within a sample. In some cases, nucleic acid-based assays can be used to assess the level of CD14.sup.+/DR.sup. cells and/or the level of CD4.sup.+ cells. For example, the amount of particular transcripts (e.g., CD14, DR, and CD4 transcripts) can be determined in whole blood using techniques such as quantitative PCR. In some cases, the ratios of cells can be used to assess a mammal's (e.g., a human's) peripheral blood phenotype. For example, the ratio of CD14.sup./DR.sup. cells to CD4.sup.+ cells (or vice versa) can be used as described herein to assess a person's peripheral blood phenotype.

[0031] In cases involving patients with glioblastoma, sepsis, or lymphoma, the determined cell levels can be compared to a cut-off value provided herein to determine whether the determined levels are normal, elevated, or reduced. In such cases, determined normal, elevated, or reduced levels can be used as described herein to classify the patient as having a likelihood to experience a favorable or unfavorable outcome. For patients with medical conditions other than glioblastoma, sepsis, or lymphoma, the level of CD14.sup.+/DR.sup. cells and the level of CD4.sup.+ cells for a population of similarly afflicted patients with known medical outcomes can be used to identify appropriate cut-off values for the CD14.sup.+/DR.sup. cell and CD4.sup.+ cell levels. In addition, the population of patients with known medical outcomes can be used to determine which combinations of cell phenotypes indicate whether a patient is likely to experience a favorable or unfavorable outcome.

[0032] Those patients determined to have a favorable or unfavorable outcome as described herein can be treated with a treatment option appropriate for their peripheral blood phenotype. For example, a patient suffering from cancer, sepsis, an autoimmune condition, or trauma who has a normal level of CD4.sup.+ cells and a normal level of CD14.sup.+/DR.sup. cells can be treated with current medical therapies for the condition to be treated such as non-immune-based therapies, radiation, chemotherapies, and/or surgery. If a patient (e.g., cancer, sepsis, an autoimmune condition, or trauma patient) has a reduced level of CD4.sup. cells and a normal level of CD14.sup.+/DR.sup. cells, then that patient can be treated with both a current medical therapy for the condition to be treated plus a T cell stimulating therapy, a CAR therapy, a DLI therapy (e.g., an allogeneic donor lymphocyte infusion therapy), a T cell stimulating antibody therapy (e.g., treatment with an anti-CTLA-4 antibody, Ipilumimab, or an anti-PD1 antibody), or a combination thereof.

[0033] If a patient (e.g., cancer, sepsis, an autoimmune condition, or trauma patient) has a normal or elevated level of CD4.sup.+ cells and an elevated level of CD14.sup.+/DR.sup. cells, then that patient can be treated with both a current medical therapy for the condition to be treated plus an anti-CD14.sup.+/HLA-CR.sup.neg therapy, a CD14.sup.+/DR.sup.neg stimulating therapy, TLR stimulating ligand therapy, a Poly I:C therapy, CpG therapy, vaccine therapy (e.g., BCG or flu vaccine therapy), an allogeneic donor lymphocyte infusion therapy, a dendritic cell infusion therapy, a cancer vaccine therapy, a CD14.sup.+DR.sup.neg killing strategy therapy, a CD14.sup.+/DR.sup.neg blocking strategy therapy, treatment with IDO inhibitors (e.g., NLG8189), treatment with arginase inhibitors, treatment with MCSF-R or CSF-R blocking agents, or combinations thereof.

[0034] If a patient (e.g., cancer, sepsis, an autoimmune condition, or trauma patient) has a reduced level of CD4.sup.+ cells and an elevated level of CD14.sup.+/DR.sup. cells, then that patient can be treated with a current medical therapy for the condition to be treated plus either (a) a T cell stimulating therapy, a CAR therapy, a DLI therapy (e.g., an allogeneic donor lymphocyte infusion therapy), a T cell stimulating antibody therapy (e.g., treatment with an anti-CTLA-4 antibody, Ipilumimab, or an anti-PD1 antibody), or a combination thereof or (b) an anti-CD14.sup.+/HLA-CR.sup.neg therapy, a CD14.sup./DR.sup.neg stimulating therapy, TLR stimulating ligand therapy, a Poly I:C therapy, CpG therapy, vaccine therapy (e.g., BCG or flu vaccine therapy), an allogeneic donor lymphocyte infusion therapy, a dendritic cell infusion therapy, a cancer vaccine therapy, a CD14.sup.+R.sup.neg killing strategy therapy, a CD14.sup.+/DR.sup.neg blocking strategy therapy, treatment with IDO inhibitors (e.g., NLG8189), treatment with arginase inhibitors, treatment with MCSF-R or CSF-R blocking agents, or combinations thereof.

[0035] The invention will be further described in the following examples, which do not limit the scope of the invention described in the claims.

EXAMPLES

Example 1

The levels of CD14.SUP.+./DR.SUP. Cells and CD4.SUP.+ Cells in Glioblastoma Patients can Predict Clinical Outcomes

[0036] Leukocytes from glioblastoma patients were analyzed by direct antibody staining of whole blood and flow cytometry. The protocol for whole blood staining was performed as described elsewhere (Gustafson et al., Neuro. Oncol., 12: 631-644 (2010)). To assess absolute cell count, 50 L of whole blood was added and stained in Trucount tubes according to the manufacturer's directions (BD Biosciences). Data was acquired on a BD FACSCalibur flow cytometer (Becton Dickinson, Franklin Lakes, N.J.) calibrated the day of use and analyzed with Cell Quest and Multiset (Becton Dickinson) software. The antibodies used included anti-CD14, anti-HLA-DR, and quantitative (Trucount) anti-CD4 antibodies. The peripheral blood monocyte phenotype (e.g., percent DR.sup. cells of CD14.sup.+ cells) was plotted against the CD4.sup.+ cell count (in cells/L) to identify cut-off values for glioblastoma patients. The patients were then categorized according to each of these values, and a survival curve was plotted.

[0037] In this example, twenty-three glioblastoma patients were phenotyped. Abnormal CD4 counts were defined as one standard deviation below the CD4 counts of normal donors (mean about 983 cells/L minus one standard deviation of 300=683 cells/L). A level of CD14.sup.+/DR.sup. cells was classified as abnormal if there were two standard deviations above the mean of the normal donor pool (about 25 or greater percent DR.sup. cells of CD14.sup.+ cells). This generated four categories:

[0038] Normal level of CD4.sup.+ cells/normal level of CD14.sup.+/DR.sup. cells (Normal; See, FIG. 1A);

[0039] Low level of CD4+ cells/normal level of CD14.sup.+/DR.sup. cells (lo DRneg, lo CD4; See, FIG. 1A);

[0040] Normal level of CD4.sup.+ cells/high level of CD14.sup.+/DR.sup. cells (no patients were found with this condition); and

[0041] Low level of CD4.sup.+ cells/high level of CD14.sup.+/DR.sup. cells (hi DRneg lo CD4; FIG. 1A).

[0042] Glioblastoma patients having normal levels of CD14.sup.+/DR.sup. cells and CD4.sup. cells experience longer survival times than glioblastoma patients in any of the other categories (FIGS. 1A-C). These results indicate that measuring immunity using these parameters predicted response to treatment, identified the best (and worst) responses to treatment, and was a useful measure of long term prognosis.

Example 2

The Levels of CD14.SUP.+./DR.SUP. Cells and CD4.SUP.+ Cells in Sepsis Patients can Predict Clinical Outcomes

[0043] Patients admitted to the intensive care unit with suspicion of bacterial sepsis (sepsis patients) were analyzed by direct antibody staining of whole blood and flow cytometry. The protocol for whole blood staining was performed as described elsewhere (Gustafson et al., Neuro. Oncol., 12: 631-644 (2010)). To assess absolute cell count, 50 of whole blood was added and stained in Trucount tubes according to the manufacturer's directions (BD Biosciences). Data was acquired on a BD FACSCalibur flow cytometer (Becton Dickinson, Franklin Lakes, N.J.) calibrated the day of use and analyzed with Cell Quest and Multiset (Becton Dickinson) software. The antibodies used included anti-CD14, anti-HLA-DR, and quantitative (Trucount) anti-CD4 antibodies. The peripheral blood monocyte phenotype (e.g., percent DR.sup. cells of CD14.sup.+ cells) was plotted against the CD4.sup.+ cell count (in cells/L) to identify cut-off values for sepsis patients (FIG. 2). The patients were then categorized according to each of these values, and a survival curve was plotted (FIG. 3).

[0044] In this example, twenty-nine patients were phenotyped. A CD4.sup.+ cell cut-off value of around 650 (mean=541; median 429) and CD14.sup.+/DR.sup. cell cut-off value of about 63% (which happens to be the mean) were used. The levels of CD14.sup.+/DR.sup. cells and CD4.sup.+ cells were classified as being elevated or reduced based on these cut-off values.

[0045] Sepsis patients having normal levels (for this patient group) of CD14.sup.+/DR.sup. cells and a normal level of CD4.sup.+ cells were likely to experience improved survival (lo DRneg Hi CD4; FIG. 3). Patients with normal CD14.sup./DR.sup. cells and a reduced level of CD4.sup.+ cells experienced an increased chance of dying (Lo DRneg Lo CD4), while sepsis patients having an elevated level of CD14.sup.+/DR.sup. cells and a reduced level of CD4.sup.+ cells (HiDRneg LoCD4) experienced an increased chance of dying (FIG. 3). There were only two patients with HiDRneg and HiCD4, and these patients were not included in the analysis.

[0046] These results indicate that peripheral blood typing of these two cell types can identify patients likely to survive using current therapy and can used as a tool to identify at risk patients.

Example 3

The Levels of CD14.SUP.+./DR.SUP. Cells and CD4.SUP.+ Cells in Lymphoma Patients can Predict Clinical Outcomes

[0047] Leukocytes from lymphoma patients were analyzed by direct antibody staining of whole blood and flow cytometry. The protocol for whole blood staining was performed as described elsewhere (Gustafson et al., Neuro. Oncol., 12: 631-644 (2010)). To assess absolute cell count, 50 L of whole blood was added and stained in Trucount tubes according to the manufacturer's directions (BD Biosciences). Data was acquired on a BD FACSCalibur flow cytometer (Becton Dickinson, Franklin Lakes, N.J.) calibrated the day of use and analyzed with Cell Quest and Multiset (Becton Dickinson) software. The antibodies used included anti-CD14, anti-HLA-DR, and quantitative (Trucount) anti-CD4 antibodies. The peripheral blood monocyte phenotype (e.g., percent DR.sup. cells of CD14.sup.+ cells) was plotted against the CD4.sup.+ cell count (in cells/L) to identify cut-off values for lymphoma patients (FIG. 4). The patients were then categorized according to each of these values, and survival curves were plotted (FIGS. 5 and 6).

[0048] In this example, twenty-eight lymphoma patients were phenotyped. A CD4.sup. cell cut-off value of around 500 and CD14.sup.+/DR.sup. cell cut-off value of about 10% were used. The levels of CD14.sup.+/DR.sup. cells and CD4.sup.+ cells were classified as being elevated or reduced based on these cut-off values.

[0049] Lymphoma patients having an increased level of CD14.sup./DR.sup. cells were likely to experience death sooner than patients with normal levels (Normal is normal levels of CD14.sup.+DR.sup.; decreased DR means loss of DR expression on CD14 or equivalent to increased CD14.sup.+DR.sup.; FIG. 6). When patients were subgrouped to include reduced or normal levels of CD4, the survival curves were only marginally changed.

[0050] These results indicate that in relapsed lymphoma patients, those patients most at risk of progression can be identified using peripheral blood phenotyping.

Example 4

An Increased Frequency of CD14.SUP.+.HLA-DR.SUP.low/neg .Monocytes Correlates with Decreased Time to Progression in Chronic Lymphocytic Leukemia (CLL)

[0051] To identify potential monocyte alterations by CLL in patients, flow cytometric analysis of peripheral blood leukocytes in patients (Table 1) with previously untreated early to intermediate stage CLL prior to therapy on a clinical trial of a therapy consisting of a five-week regimen of alemtuzumab, rituximab, and GM-CSF was performed, and their progress was followed through twelve months (ClinicalTrials.gov NCT00562328). Antibody staining of whole blood and flow cytometry data collection were performed as described elsewhere (Gustafson et al., Neuro. Oncol., 12:631-644 (2010)). In healthy individuals, about 90% of circulating CD14.sup.+ monocytes were positive for surface HLA-DR. The percentage of leukocytes that were monocytes in CLL patients were similar to those seen in healthy volunteers. However, the CD14.sup.+ monocytes in CLL patients were more likely to have reduced staining for HLA-DR than age-matched healthy volunteers (16.8% 11.5% vs. 9.9% 6.4%, p=0.008) (FIG. 7). The expression of monocyte activation markers CD16, TNFR2, and CD80 were similar in the CLL patients and healthy volunteers. However, CD86 expression on monocytes was decreased in CLL patients versus healthy volunteers (83.9% 17.0%; n=9 vs. 94.9% 1.2%; n=5; p=0.0290). The diminished expression of HLA-DR and CD86 molecules suggested that the monocytes in CLL patients could have decreased antigen presenting capacity with reduced immune stimulatory capacity.

TABLE-US-00001 TABLE 1 Patient Characteristics. Age, median (range) 59.0 (42.0-77.0) Gender Female 8 (27.6%) Male 21 (72.4%) Follow up Status Alive 28 (96.5%) Dead 1 (3.5%) Median Follow-up (months) 26.8 (10.1-38.8) Progression Status No progression 11 (37.9%) Progression 18 (62.1%) Rai Stage 0 2 (6.9%) 1 23 (79.3%) 2 4 (13.8%) CD38+ Expression Positive 14 (48.3%) Negative 15 (51.7%) IgVH Mutation Mutated 3 (10.3%) Unmutated 26 (89.7%) Zap-70 Expression Positive 21 (75%) Negative 7 (25%) FISH, abnormal (24, 82.8%) 13q14 4 (13.8%) 12+ 6 (20.7%) 11q22 10 (34.5%) 17p13 3 (10.3%) Other 1 (3.5%) Normal 5 (17.2%)

[0052] The relationship between the pre-treatment monocytes, CD14.sup.+HLA-DR.sup.log/neg cells, and CD19.sup.+ B cell (predominantly CLL cells) counts was also studied. For these comparisons, the percentage of CD14.sup.+HLA-DR.sup.lo/neg cells or monocytes was converted into cells/L. A positive correlation between the numbers of B cell and monocyte (p<0.0001) and increased numbers of CD14.sup.+HLA-DR.sup.lo/neg cells (p=0.0009) was identified. It was investigated whether a sustained reduction in the absolute B cell count after treatment would be associated with a normalization of the immune profile in terms of the monocyte pool. In patients who were in sustained remission at 12 months after completion of therapy (n=18), the median frequency of CD14.sup.+HLA-DR.sup.lo/neg monocytes decreased (17.9% 12.3% pretreatment vs. 9.9% 10.0% post-treatment, p=0.0046, FIG. 7; upper right) to a value similar to healthy volunteers. This was not due to selection bias as there was no difference between the pretreatment frequency of CD14.sup.+HLA-DR.sup.lo/neg monocytes in patients with a sustained 12 month response compared to patients without this response. These results supported a model also observed in glioblastoma of tumor mediated changes in monocyte phenotype and suggest that loss of the tumor signal may lead to reversion to a normal phenotype.

[0053] To determine if monocyte phenotypes were prognostic, the time to disease progression in patients with elevated pretreatment frequency of CD14.sup.+HLA-DR.sup.lo/neg monocytes (2.5 standard deviations above the healthy volunteer mean) was compared to those with lower levels of CD14.sup.+HLA-DR.sup.log/neg monocytes. The 6 patients with higher CD14.sup.+HLA-DR.sup.lo/neg monocytes exhibited a shorter time to disease progression (median 6.9 months) compared to 19.1 months for patients with lower levels (n=22; p=0.024, FIG. 7; lower panel). The number of total monocytes did not influence time to disease progression. These data suggest loss of DR expression by CD14 cells is predictive of poorer prognosis.

[0054] CD14.sup.+HLA-DR.sup.lo/neg cells mediate immunosuppression through secretion of IL-10 and/or TGF-, can induce T regulatory populations, inhibit responder T cells, and have defects in dendritic cell maturation. There is also growing evidence that nurse-like cells are derived from CD14.sup.+ cells. Monocytes likely play a dual role in CLL of promoting CLL survival and mediating CLL-induced immunosuppression reflecting the importance of myeloid cell interaction on the pathogenesis of CLL. The elevated frequency of CD14.sup.+HLA-DR.sup.lo/neg monocytes and their association with increased tumor burden and poorer prognosis suggested an important role of monocytes in the pathogenesis of CLL. Taken together, these results demonstrate that the level of CD14.sup.+HLA-DR.sup.lo/neg monocytes can be used to determine prognosis and potentially classify patients into various risk groups.

Example 5

An Increased Frequency of Peripheral Blood CD14.SUP.+.HLA-DR.SUP.low/neg .Monocytes Correlates with Increase CD14.SUP.+ Tumor Infiltration and Poorer Prognosis in Renal Cell Carcinoma

[0055] The following was performed to assess the associations of tumor CD14 expression with clinical and pathologic features and patient outcome using a large cohort (n=375) of ccRCC patients. The association of maximal intratumoral and peritumoral CD14 expression with cancer-specific survival is illustrated in FIG. 8A. At last follow-up, 159 patients had died, including 100 who died from RCC at a mean of 2.3 years following surgery (median 1.7; range 0-9). Among the 216 patients who were still alive at last follow-up, the mean duration of follow-up was 7.1 years (median 7.3; range 0-10); only 5 (2.3%) patients had fewer than 2 years of follow-up. Estimated cancer-specific survival rates (95% CI, number still at risk) at 1, 3, 5, and 7 years following surgery were 91.0% (88.1-94.0; 328), 79.0% (74.9-83.4; 268), 75.3% (70.9-80.0; 232), and 71.9% (67.3-77.0; 136), respectively. Univariately, patients whose tumors contained moderate CD14 expression were nearly 5 times more likely to die from RCC compared with patients whose tumors contained absent/focal CD14 expression (HR 4.79; p<0.001). Patients whose tumors contained marked CD14 expression were over 11 times more likely to die from RCC compared with patients whose tumors contained absent/focal CD14 expression (HR 11.51; p<0.001). These associations also were evaluated in a multivariable setting adjusting for the SSIGN score. After accounting for the association between SSIGN score and death from RCC, the HRs for the associations of moderate and marked CD14 expression with death from RCC were 2.87 (p<0.001) and 3.03 (p<0.001), respectively. After further adjustment for age at surgery, gender, symptoms at presentation, sarcomatoid differentiation, and the SSIGN score, the HRs for the associations of moderate and marked CD14 expression with death from RCC were 2.53 (95% CI 1.45-4.42; p=0.001) and 2.69 (1.44-5.01; p=0.002), respectively. Since it is technically difficult to assess changes in HLA-DR levels by immunohistochemistry, the tumors were stained for CD14 from the 23 ccRCC patients that were immunophenotyped for CD14 and HLA-DR. It was found that the HLA-DR expression on peripheral blood CD14.sup.+ monocytes in ccRCC patients inversely correlated with the intensity of CD14 staining in their corresponding tumors (FIG. 8B). Taken together, these results reveal that the level of peripheral blood CD14.sup.+HLA-DR.sup.lo/neg monocytes can be a surrogate measure of the amount of CD14.sup.+ monocytes in the tumor and that their presence in tumors predicts patient survival.

Example 6

HLA-DR Protein Expression Correlates with HLA-DR mRNA Expression

[0056] Paired blood samples from healthy volunteers and cancer patients were analyzed by flow cytometry and quantitative PCR (QPCR). RNA was isolated using the Qiagen RNeasy Plus kit. cDNA and QPCR with TAQMAN probes were performed and analyzed via the Roche Light Cycler 2.0 System. Primers were designed via Roche online tools. Crossing Point (CP) is the threshold in which a gene detected above background. For flow cytometry, cells were stained with appropriate antibodies at RT for 15 minutes, washed in PBS, and fixed in 4% paraformaldehyde. Data were acquired on a FACS Calibur Flow Cytometer and analyzed using CellQuest software. The percentage of CD14.sup.+HLA-DR.sup.lo/neg monocytes was plotted against the crossing point of HLA-DR expression from each individual (FIG. 9).

[0057] Taken together, these results demonstrate that there is a significant correlation between HLA-DR surface expression and transcript amounts suggesting that Q-PCR may be used as an interchangeable technique to flow cytometry in the understanding of the immune biology.

Other Embodiments

[0058] It is to be understood that while the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate and not limit the scope of the invention, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims.