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Conceived and designed the experiments: SMK DRS. Performed the experiments: YAG SMK DC. Analyzed the data: YAG SMK JD ABK. Contributed reagents/materials/analysis tools: ZA DB JS TN AQ HS SLP RLS JSF TM SRH SMF ABK CLM. Wrote the paper: YAG DRS.
A major challenge for the field of transplantation is the lack of understanding of genomic and molecular drivers of early post-transplant immunity. The early immune response creates a complex milieu that determines the course of ensuing immune events and the ultimate outcome of the transplant. The objective of the current study was to mechanistically deconvolute the early immune response by purifying and profiling the constituent cell subsets of the peripheral blood. We employed genome-wide profiling of whole blood and purified CD4, CD8, B cells and monocytes in tandem with high-throughput laser-scanning cytometry in 10 kidney transplants sampled serially pre-transplant, 1, 2, 4, 8 and 12 weeks. Cytometry confirmed early cell subset depletion by antibody induction and immunosuppression. Multiple markers revealed the activation and proliferative expansion of CD45RO+CD62L− effector memory CD4/CD8 T cells as well as progressive activation of monocytes and B cells. Next, we mechanistically deconvoluted early post-transplant immunity by serial monitoring of whole blood using DNA microarrays. Parallel analysis of cell subset-specific gene expression revealed a unique spectrum of time-dependent changes and functional pathways. Gene expression profiling results were validated with 157 different probesets matching all 65 antigens detected by cytometry. Thus, serial blood cell monitoring reflects the profound changes in blood cell composition and immune activation early post-transplant. Each cell subset reveals distinct pathways and functional programs. These changes illuminate a complex, early phase of immunity and inflammation that includes activation and proliferative expansion of the memory effector and regulatory cells that may determine the phenotype and outcome of the kidney transplant.
A major challenge for the field of transplantation is the lack of understanding of genomic and molecular drivers of early post-transplant immunity. The early inflammatory response is initiated by ischemia/reperfusion, activation of innate immunity and subsequent alloantigen-primed T cell recruitment, activation and proliferative expansion –. The early immune response creates a complex milieu that contributes significantly to the course of ensuing events and the ultimate outcome of the transplant including acute and chronic rejection –. Thus, profiling the mechanisms of early immunity is essential.
The last several decades of evolving clinical practice in kidney transplantation has focused on increasing graft survival by reducing the risk of acute rejection, while enhancing the safety profiles of the drug regimens employed , . It is now common to use induction therapy with anti-lymphocyte antibody preparations to profoundly deplete the cellular immune system immediately at the time of transplantation –. Induction in combination with current drug therapies reduces acute rejection incidence to less than 15% in the first year , . Unfortunately, these dramatic results in the short term reduction of acute rejection have not directly translated to long term immune tolerance with successful drug withdrawal or even a significant reduction in the incidence of chronic rejection or chronic allograft nephropathy with interstitial fibrosis and tubular atrophy (CAN/IFTA) –. Moreover, several studies in which biopsies were performed by protocol rather than by clinical indication between 6 and 12 months after transplantation revealed that up to 15% of patients demonstrated evidence of an active immune/inflammatory response despite no evidence of transplant dysfunction , . Thus, there is a pressing medical need to understand what changes evolve in this early post-transplant period that allows the immune response to reemerge intact and target the transplant for immune-mediated rejection and injury.
The objective of the current study was to mechanistically deconvolute the early immune response in kidney transplant patients after antibody induction therapy by purifying and profiling the constituent peripheral blood cell subsets using two complementary technologies. First, we employed the novel SurroScan™ laser scanning cytometry , ,  technology on whole blood cell populations to create a comprehensive survey of well-established cell surface marker expression from 10 consecutively enrolled transplant patients and 5 healthy controls. The transplant patients were serially sampled from pre-transplant (Pre-TX) to 12 weeks post-transplant (Post-TX). Second, genome-wide differential gene expression profiling was done. We purified and analyzed CD4+ and CD8+ T lymphocytes, CD14+ monocytes, and CD19+ B cells. Whole blood and subset-specific gene expression profiles were used to populate and map molecular pathways as a function of time and population.
This novel approach to cell subset-based deconvolution revealed the profound changes in blood cell composition and the activation of multiple molecular pathways that occurs early Post-TX. Moreover, each immune cell subset revealed a distinct set of pathways and functional programs. Indeed, these subset-specific changes illuminate a complex, early phase of alloimmunity characterized by the activation and proliferative expansion of the memory effector and regulatory T cells that play major roles in determining the outcome of the kidney transplant. We also demonstrated significant activation and proliferative expansion of CD14 monocytes that are linked to ischemia reperfusion injury, innate immunity and the transition to adaptive immunity. Finally, we demonstrated the progressive activation of B cells by 12 weeks consistent with early recruitment of the humoral immune system post-TX.
Table 1 presents the clinical characteristics collected from 10 kidney transplant patients. Five patients were converted to sirolimus immunosuppression at 12 weeks, two patients experienced acute rejection episodes at 7 and 10 months, and creatinine levels out to 12 months are provided. All patients were enrolled in a single, consecutive series after consent. Table 2 lists all the samples obtained for this study.
A primary objective was to determine differences in immune/inflammatory cell populations in the early Post-TX period. SurroScan™ microvolume laser scanning cytometry provides quantitative measurements of absolute cell counts per microliter of blood and simultaneous measurement of hundreds of cell surface markers defining multiple cell populations . Of 1083 variables measured at each time point, 441 were significantly different at week 1 and 259 at week 12 (p<0.01) (Table 3).
Thymoglobulin induction also causes a rapid and profound reduction in multiple cell populations –. The changes in absolute cell counts for each major cell population are given in Figure 1A. Consistent with a previous report following longer term cell reconstitution , T cell counts returned to only 20% of Pre-TX levels at 12 weeks and CD4 levels lagged behind CD8. The excellent correlations of T cell markers with the gene expression data we will describe later demonstrate the first proof for integrating cytometry and DNA microarray profiling (Figure 1B).
The distribution of different CD4 T cell subsets evolved from Pre-TX to 12 weeks (Table 4). Naïve and memory CD4 subsets differ by expression of CD62L and either CD45RO (memory) or CD45RA (naïve). At 12 weeks, there was a significant expansion of memory effector CD4 cells (CD45RA−CD62L) from 30% Pre-TX to 45% at 12 weeks (p<0.01). These memory effector CD4 also significantly increased their expression of multiple activation markers: CD60 , CCR5 (CD195) , CD69 , CD86 , CD132 , CD27  and HLA DR . While the CD4+CD25+ T cells are also depleted by induction, they increased significantly (2.5-fold) by 12 weeks. Reciprocally, the naïve CD4 population was significantly lower at 12 weeks, going from 28% to 12% of the total CD4 T cells (p<0.001). In contrast, there were no significant changes in central memory or terminal effector CD4 numbers.
By 12 weeks total CD8 cells were 40% of baseline (Figure 1A). Parallel to the CD4 data, there was an observed increase in activated memory effector CD8 cells (CD45RA−CD62L−; 25% to 30%; Table 4). While this did not reach statistical significance, the parallel increase in CD8+CD45RA− cells from 35% to 42% was significant (p<0.05). Multiple activation markers were also upregulated on CD8 including CD60, CCR5, CD27, while CD25 and CD57-expressing subsets were decreased by 25–50% at 12 weeks. In contrast to CD4, there was a significant decrease in terminal effector CD8 T cells from 35% to 23% (p<0.05).
B cells and monocyte numbers dipped between weeks 1 and 4 but recovered to near baseline by 12 weeks (Figure 1A). Cell counts were well correlated to gene expression for B cell markers (CD19-21 and CD72; data not shown), another benchmark for integrating cytometry and gene expression. B cells expressing the activation marker CD38 were significantly higher 12 weeks Post-TX going from 31% to 45% (p<0.05; Table 5), consistent with the role for this molecule in responses to T cell dependent protein antigens . In addition, B cells also demonstrated a significant increase of cells expressing the activation markers CD5, CD40, CD95 between early and late (data not shown). The number of monocytes in whole blood was also significantly higher by week 12 (2.1–2.4 fold; Table 5) and the TLR2+ (CD282) population also increased. Additional evidence for B cell and monocyte activation post-transplant are the progressive increases in HLA expression in both peaking at week 12 (Figure 2).
Differential gene expression for each Post-TX timepoint was determined. In a second analysis, ANOVA comparisons were done for all timepoints to determine genes that change in a coordinate fashion as a function of time (e.g. multivariate genes). These two analysis strategies are intended to be complementary. The number of differentially expressed genes obtained in each whole blood cell analysis is provided in Figure 3A and Table 6. The total number of differentially expressed and percent upregulated genes was highest at week 1 (2638; 20.4%) and decreased progressively by week 12 (1148; 6.7%). By ANOVA, we found 2447 multivariate genes, whose expression evolves in the continuum from Pre-TX to week 12. The majority of multivariate genes (90%) were also downregulated Post-TX (Table S1).
Next, we performed a functional analysis of gene expression comparing the Pre-TX gene expression to each of the serial time points sampled. We populated all possible functional pathways and then extracted only statistically significant pathways (p<0.05; Methods S1) for further analysis. Four classes of functional pathways were populated by this analysis: early (1–4 weeks), late (8–12 weeks), consistent (all timepoints) and intermittent (selected timepoints) (Figure 3B).
Most pathways were populated either early or consistently (see Table S2 for gene details). Early pathways included NK Cell Signaling, CD1 Lipid Antigen Presentation and mTOR Signaling. Consistently populated pathways included CTLA4 Signaling in CTL, TCR Signaling, iCOS-iCOSL Signaling and CD28 Signaling. It is evident that these pathways include many of the known primary mechanisms of alloimmunity – and a key finding is that the majority of the genes populating these pathways are downregulated in the first 12 weeks coinciding with antibody induction and immunosuppression.
Using the 2447 multivariate genes by ANOVA, we populated 19 significant functional pathways with 134 significantly differentially expressed genes (Figure 3C, Table S3). These genes populate a combination of immune response and metabolic pathways. The top 5 pathways are CTL-mediated apoptosis (35.7% populated), aminoacyl-tRNA biosynthesis (27.5% populated), glutamate metabolism (21.6% populated), alanine and aspartate metabolism (21.4% populated), and allograft rejection signaling (20.5% populated).
Two comparisons were done: Pre-TX vs. week 2 (early) and Pre-TX vs. week 12 (late). Pre-TX vs. week 2 revealed 1584 significantly differentially expressed genes. In sharp contrast to what was found by whole blood analysis, 45.8% of these CD4+ genes were upregulated (Table 6). Pre-TX vs. week 12 revealed 3358 genes differentially expressed of which 50.1% were upregulated. Thus, by week 12, the total number of differentially expressed and upregulated genes more than doubles in the CD4+ T cells.
Functional pathways were mapped to understand changes in differential gene expression between early and late Post-TX by the strategy shown in Figure 4A. It is evident that there are many unique pathways populated by genes expressed in either the early or late phase (Figure 4B). For example, VEGF, IGF1, chemokine, apoptosis and hypoxia signaling are unique early phase responses while CD28, angiopoietin, IL2, IL15 and Fce R1 signaling are unique in the late phase. Second, a large number of pathways are shared by both phases. However, it is important to note that these pathways are consistently populated by increasing numbers of differentially expressed genes in the late phase. These represent functional pathways triggered in the early phase that clearly are evolving with new gene members of the pathways being recruited and activated in the late phase of the immune response post transplant.
Class comparisons of CD8 populations yielded 574 differentially expressed genes between Pre-TX and week 2 (51.3% upregulated) and 2030 genes between Pre-TX and week 12 (54.2% upregulated) (Table 6). Thus, the number of differentially expressed CD8+ genes almost quadruples by week 12.
Comparison analysis identified pathways populated either early, late or at both phases Post-TX (see Table S4 for entire list of pathways). The majority of pathways were either uniquely populated in the early phase (52 pathways) or expressed during both phases (46 shared pathways) compared to only 22 unique late pathways. The top 66 populated pathways are shown in Figure 5. Second, as seen with the CD4+ T cells, every shared pathway demonstrates a significant increase in the number of populating genes from week 2 to 12. Unique early pathways include IL2, IL4, sphingosine-1-phosphate and CD27 signaling. Unique late pathways include fatty acid biosynthesis, chemokine, Wnt-catenin, cell cycle signaling and IL15 production. Shared pathways increasingly populated in the late phase include IL3, CD28, integrin, VEGF and IL15 signaling, the latter matching the IL15 production pathway seen only in the late phase.
Because of low cell yields, we substituted CD14-purified normal donor controls for the Pre-TX baselines and normalized the data by eliminating any genes differentially expressed between the controls and the two Pre-TX samples available. The class comparison at week 2 yielded 312 differentially expressed genes, 258 of which remained after normalization (84% upregulated; Table 6). At week 12, we identified 616 genes, 455 of which remained after normalization (54% upregulated).
Mapping of functional pathways demonstrates a distinct contrast with the CD4 and CD8 results. In the CD14 subset, pathways are uniquely populated in the early (27 pathways) or the late phase Post-TX (17 pathways) with only 2 common pathways (PTEN and HMGB1 signaling) (Figure 6A). The nature of these CD14 pathways is also distinct between early and late. A large number of immune/inflammatory cytokine signaling and TLR pathways are activated early. Multiple metabolic and synthetic pathways are populated late consistent with the proliferative expansion of the activated CD14 phenotype demonstrated by cytometry.
Again, due to low cell yields, CD19 profiling was performed substituting normal donor controls for Pre-TX samples and normalizing. Class comparisons identified 208 significant differentially expressed genes at week 2 (58.1% upregulated) and 389 genes (49.1% upregulated) at week 12 (Table 6). Functional mapping populated 32 total pathways (Figure 6B) of which only 10 are populated early and 20 are late. Late pathways are rich in immune signaling pathways: interferon, IL2, integrin, PKR-interferon induction, PDGF, TLR receptors, and communications between innate and adaptive immunity. Only two pathways are shared but highly populated: IL9 signaling, a cytokine made by activated T cells, and RAN signaling linked to transport of RNA and proteins from the nucleus.
There is a significant difference in the percent of up/downregulated genes identified by whole blood analysis (11% upregulated; week 2) and the purified CD4, CD8 and CD14 analyses (46%, 52% and 84% upregulated) (Figure S1 A and B). The majority of differentially expressed genes in all comparisons are unique to either whole blood or the individual cell subsets underlining the extent of additional information provided by subset analysis in this situation. Secondly, few genes in the subsets move coordinately in opposite directions from whole blood indicating that these values would not cancel out when analyzed in a whole blood sample. As shown in Figure 1, cytometry reveals a dramatic depopulation of the major lymphocyte populations immediately following antibody induction therapy. Thus, the explanation for these huge differences in gene expression between whole blood and purified subsets is the impact of the high numbers of neutrophils, eosinophils, and basophils remaining in whole blood.
Finally, we tested whether we could proteogenomically validate the results of both cytomety and gene expression. We matched 157 different DNA array probesets used for gene expression profiling to the 65 different cell proteins tested by specific antibodies and cytometry. Thus, the novel premise is that the gene expression array data is validated proteomically by the cytometry and the protein expression data identified by cytometry is validated by the gene expression profiling. We found that all the gene expression calls and all the proteins identified were detected by both technologies (Table S5).
We have used two complementary strategies to deconvolute the early post-transplant immune response. The first is based on a novel high-throughput laser scanning cytometry technology enabling hundreds of parallel analyses in whole blood . The second approach was purifying constituent blood cell subsets followed by genome-wide gene expression profiling. We studied 10 consecutive kidney transplants with serial blood samples analyzed pre-transplant and at 1, 2, 4, 8 and 12 weeks. Our results provide a unique view of the complex evolution of immune/inflammatory molecular pathways occurring early post-transplant. A critical finding is that the constituent blood cell subsets reveal an entirely new level of detail, effectively deconvoluting a process that is otherwise lost in the mix. A second critical finding is that even in this early period post-TX during the most intense immunosuppression there emerges a clear pattern of immune activation involving memory T cells, monocytes and B cells.
Cytometry results demonstrate the profound reductions in lymphocyte subsets expected with antibody induction. Nonetheless, we demonstrate significant increases in memory CD4 effector cells (CD45RA−CD62L−) and a reciprocal decrease in naïve CD4, consistent with previous reports , , . These results support the hypothesis that the protective impact of induction therapy may be limited in this early period by the relative resistance and subsequent expansion of memory effector CD4 cells. In fact, the expansion of memory effector CD4 is supported by the significant upregulation of multiple activation markers. Additionally, induction is less effective at CD8 depletion and these cells also express multiple activation markers and recover more rapidly . The significant reduction in the CD8 terminal effector cell population (CD45RA+CD62L−) in the context of activation indicates that this early proliferation favors CD8 effector memory and central memory subsets.
A reasonable question is whether cytometry and gene expression data correlate, in effect allowing a proteogenomic validation of both results consistent with our view that these technologies are complementary. Comparison of cytometry and gene expression for multiple pan T cell markers such as CD3e,g,d, TCRab, CD2, CD5, CD6 and CD7 correlated well and similar results were found for pan B cell markers. In fact, gene expression profiling results were validated with all 65 protein antigens measured by cytometry at multiple time points. In turn, all 65 proteins were validated with 157 different probesets detecting the corresponding mRNA transcripts on DNA microarrays. Thus, microarray-based gene expression is representative of the cell proteins expressed and this represents a novel strategy for validating gene expression results by cytometry-based proteomics.
We next investigated gene expression profiles obtained from whole blood. Given the availability of reagents enabling whole blood transcriptome analysis in a clinical setting it was logical to start here. Functional analysis was done using a curated and constantly updated literature database (Ingenuity Pathways Analysis) to populate known pathways with significantly differentially expressed genes. Four classes of functional pathways were populated in the first 12 weeks post-TX: early (1–4 weeks), late (8–12 weeks), consistent (populated at all timepoints) and intermittent (selected timepoints). Most of the pathways were populated either early or consistently and related to primary mechanisms of alloimmunity –. Thus, even in this complicated period, by looking at the evolution of the changes in whole blood gene expression, we identified 2447 genes that change uniquely as a function of time and these mapped to 19 canonical functional pathways (Figure 3C). The obvious question is what do we miss in a whole blood analysis because of the dramatic changes in the cell composition that occur after antibody induction in this early period.
The immediate impact of induction is a profound depletion of CD4, CD8 and NK cells, while B cells, eosinophils and neutrophils are suddenly the dominant populations. The ideal way to address this confounding cell admixture challenge is to separate the constituent cell subsets and analyze gene expression from each. We have reviewed in detail the results of these studies. These cell subset-specific results reveal a number of new insights into the mechanisms that may drive the early Post-TX immunity, and are not revealed by whole blood analysis. For example, as shown in Figure 4B, we have defined unique early, late and shared pathways for CD4 T cell activation Post-TX. These shared pathways are consistently populated by increasing numbers of differentially expressed genes in the late phase, revealing pathways that are triggered early and then evolve by recruitment and activation of new genes into each pathway with time.
Results for CD8, CD14 and CD19 subsets also demonstrate the evolution of distinct molecular networks as a function of time and cell subset. For example, most of the genes and pathways identified for CD8 are not common to those identified for CD4, underlining the unique nature of the mechanisms driving activation and proliferative expansion of these two T cell subsets. Pathway analysis for CD14 monocytes is consistent with our data showing upregulation of activation markers and published literature that early Post-TX events are dominated by ischemia/reperfusion injury and activation of innate immunity , , . Thus, the majority of CD14 pathways are activated in the early phase and include signaling via IL10, PPAR, APRIL, ICOS and TLR. In contrast, the majority of CD19 pathways are populated only in the late phase of the early immune response including signaling via: IL9, interferon, IL2, CD4 differentiation, PKR-interferon induction and TLR receptors. Whether these represent coordinated waves of signaling from monocytes to B cells during this early activation of transplant immunity will have to be tested.
This study has several limitations that are important to acknowledge. The data is limited to only 10 patients and 5 healthy donors. To mitigate sample size limitation, patients were enrolled consecutively to avoid selection bias. Also, the serial time sampling of whole blood and purified cell subsets presented here represents over 170 microarrays and thousands of parallel cytometry measurements. Stopping the study at 12 weeks was arbitrary. We also acknowledge that our use of the terms early and late, refer to this 12 week period, which is certainly early in the post-transplant course. The immune response continues to evolve as a function of time and critical events can and will occur later. Future studies, based on the proof of concept provided here, can explore that question productively for the entire first post-transplant year.
There is no attempt to identify specific genes or biomarkers for early transplantation. And the small numbers of patients studied in this pilot preclude any outcome-specific correlations. Rather, we are clear that this study was designed to test the hypothesis that deconvolution of the early Post-TX period is possible by analysis of purified blood cell subsets. First, the results demonstrate that even without subset purification there is considerable information contained within the genome and cytometry data of whole blood samples to identify a number of important candidate pathways. Second, subset-based deconvolution allows a novel correlation of the profound changes in blood cell composition created by antibody induction with the molecular pathways activated in critical immune cell subsets. These subset-specific changes illuminate a very complex, early phase of immunity that includes activation and proliferative expansion of the memory effector and regulatory cells that determine the phenotype and outcome of the kidney transplant. In fact, it is striking that in this first 12 weeks under the most intense levels of immunosuppression achieved at any time post-transplant that there is such a dramatic activation of CD4, CD8, CD14 and B cells and particularly of the memory effector subsets. With these results, it is now justifiable to consider a larger investment in serial sampling and blood cell subset analysis of kidney transplant patients that should extend its reach to at least 12 months post-transplantation. Ultimately, the question for the field is whether these networks of immune activation represent the necessary repopulation of the immune system in response to early antibody-mediated destruction, and if so, what are the implications of this activation for the evolution and regulation of the post-transplant immune response? The current clinical reality is that despite significant reductions in the incidence of acute rejection over the last two decades, we still have not found a protocol that results in tolerance with drug withdrawal or even indefinite long term graft survival on immunosuppression.
All the studies in this manuscript were covered by Human Subjects Research Protocols approved by the Center's Institutional Review Board and by the IRB of The Scripps Research Institute. Informed written consent was obtained from all study subjects in the study.
The immunosuppressive protocol was: methylprednisolone (60 mg/days 1–4); rabbit polyclonal anti-thymocyte globulin (Thymoglobulin®; 6 mg/kg in 3 doses); mycophenolate mofetil (CellCept®); and tacrolimus (Prograf®). Peripheral blood from 10 transplant patients was collected with IRB approved informed consent at the Scripps Center for Organ and Cell Transplantation immediately prior to administration of immunosuppression and transplantation and at weeks 1, 2, 4, 8, and 12. Whole Blood was collected into PAXgene (PreAnalytix, Franklin Lakes, NJ) or EDTA-coated tubes for separation into cell subsets using positive cell selection with magnetic Dynal beads (Invitrogen, Carlsbad, CA). Blood Samples from 5 healthy control subjects from our Normal Blood Drawing Service represented by 2 males and 3 females, 25–45 years of age, were collected following the same protocol at a single time point.
Cytometry analysis was performed on the SurroScan™ system (SurroMed/PPD Biomarker Discovery Sciences) comprised of 49 three-color cell surface assays performed by microvolume laser scanning cytometry as described previously –, . Template gates were established using FlowJo™ software (Tree Star, Inc., Ashland, OR) customized for PPD. Gating information was applied for each assay using CytoSuite™ analysis software to generate cell counts and antigen intensity data. Table S6 provides a summary of target antigens used in this study for each major cell population. Template gates were established with healthy controls (Stanford Blood Bank) and confirmed to work with study samples (Figure S2). Control experiments demonstrated that residual thymoglobulin did not interfere with the cytometry measurements (not shown). We evaluated 1083 statistical variables from cell counts and cell surface antigen intensities. Within group comparisons were performed as paired two-group comparisons to identify differences associated with transplantation and immunosuppression independent of outcome. If all variables were independent, 11 would be expected to be different by chance at a univariate p-value of <0.01.
RNA was extracted and hybridized to Affymetrix U133 Plus 2.0 GeneChips (Affymetrix, Santa Clara, CA). Normalized signals were used for class comparisons of variance by two-way t-tests for two sample comparisons and parametric univariate F-tests for multiple sample comparisons (p<0.001, FDRs<2%; BRB-ArrayTools, (http://linus.nci.nih.gov/BRB-ArrayTools.html) to identify significantly differentially expressed genes. All tests done were based on comparing the differences in normalized, mean log-transformed intensities between classes of samples. Heatmaps were generated using Cluster and Treeview . Functional mapping was performed using Ingenuity Pathway Analysis (IPA, Ingenuity® Systems, Redwood City, CA, http://www.ingenuity.com). All gene expression files are available at the NIH GEO site, submission number GSE24223. For detailed description of cytometry, statistical methods and gene analysis refer to Methods S1.
Comparisons of gene expression between 3 cell subsets (CD4, CD8 and CD14) and whole blood. (A) The Venn diagram represents the gene expression overlaps between whole blood (WB) and the purified CD4, CD8, and CD14 subsets, showing genes downregulated early. The number in parenthesis next to each cell subset represents the total number of downregulated genes at that timepoint Post-TX. The data shows that the majority of genes differentially expressed early in each cell type is unique to that cell type. (B) The Venn diagram represents the gene expression overlaps between whole blood (WB) and the purified CD4, CD8, and CD14 subsets, showing genes downregulated late in the 12 week period post transplantation. The number in parenthesis next to cell subset represents the total number of downregulated genes at that timepoint Post-TX. The data shows that the majority of genes differentially expressed late in each cell type is unique to that cell type.
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Representative laser scanning cytometry plots with standard gates for the major cell populations. (A) Total T cells identified with CD3; (B) CD4 and CD8 T cells after gating on CD3; (C) NK cells identified as CD3 negative (not shown) and CD2 and CD56 positive; (D) B cells (CD20) and monocytes (CD14); (E) Granulocytes (CD16) and monocytes (CD14); and, (F) granulocytes (CD16) and eosinophils, identified as CD16 negative and CD66b positive. All of these examples are from whole blood staining with healthy controls. When a population was measured in more than one assay, averages of the absolute cell counts were used for the comparative statistics.
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Whole Blood multivariate gene expression
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134 multivariate whole blood genes that populate 19 significant functional pathways
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Significant pathways (p<0.05) identified in Ingenuity Pathway Analysis populated by genes from whole blood as a function of the serial time points sampled
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Comparison analysis of functional pathways populated either early, late or at both stages Post-Tx in CD8 subset
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Cytometry Antigen Gene Expression
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Target Antigens for Cellular Assays.
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We acknowledge the unselfish contributions of all the patients and healthy normal donors that provided samples for this research. We also appreciate the hard work and dedication of the clinical nurses and physician assistants at the Scripps Center for Organ and Cell Transplantation that made this work possible.
Competing Interests: There are two competing interests involved in this study. 1) Roche Pharmaceuticals employed the following authors: Z. Avnur, D. Borie, T. Nikolcheva, A. Quinn, and S.L. Peng. Roche funded part of this work as an unrestricted research grant to Dr. Daniel R. Salomon, the senior author. The rest of the work was supported by NIH grant AI063603 to Dr. Salomon. These employees of Roche were scientific collaborators and involved in the development of the study design and reviewed the first part of the data generated. Roche has relinquished any patent interests or IP ownership in anything involved in this project. Dr. Salomon and his collaborating scientists at Scripps and The Cleveland Clinic have no ongoing consultant or speaker arrangements of any kind with Roche and no stock, stock options or other forms of equity in Roche. 2) PPD employed the following authors during the time this work was done: J. Deng, A.B. Kantor, and H. Schulman. PPD provided the Surroscan high throughput flow cytometry work in the manuscript and their participation was funded by Roche as a combination of fee for service, and then consultant fees for the data evaluation and presentation phase of the Roche-funded portion of the work. PPD has never had any patent, IP or other rights in this work. These competing interests do not alter the authors' adherence to all the PLoS ONE policies on sharing data and materials as outlined at the journal website online.
Funding: NIH U19 AI063603, Molly Baber Research Fund, Verna Harrah Research Fund, service work for high throughput flow cytometry and data analysis by Pharmaceutical Product Development Inc. (PPD) and an unrestricted research grant from Roche Pharmaceuticals. Roche and PPD were involved in the study design as a scientific collaboration and involved in the first half of the data collection and analysis that was performed during the period covered by their unrestricted educational grant. Roche and PPD were not involved in the next stage, where the second half of the samples were analyzed and in all the subsequent data analysis, genomic pathway mapping, final decision to publish, and preparation of the manuscript. The Roche and PPD authors as listed, however, were treated as scientific collaborators and were provided a full copy of the submitted manuscript for their review and approval prior to submission.