Personalized medicine in psoriasis: developing a genomic classifier to predict histological response to Alefacept
© Suárez-Fariñas et al; licensee BioMed Central Ltd. 2010
Received: 29 June 2009
Accepted: 12 February 2010
Published: 12 February 2010
Alefacept treatment is highly effective in a select group patients with moderate-to-severe psoriasis, and is an ideal candidate to develop systems to predict who will respond to therapy. A clinical trial of 22 patients with moderate to severe psoriasis treated with alefacept was conducted in 2002-2003, as a mechanism of action study. Patients were classified as responders or non-responders to alefacept based on histological criteria. Results of the original mechanism of action study have been published. Peripheral blood was collected at the start of this clinical trial, and a prior analysis demonstrated that gene expression in PBMCs differed between responders and non-responders, however, the analysis performed could not be used to predict response.
Microarray data from PBMCs of 16 of these patients was analyzed to generate a treatment response classifier. We used a discriminant analysis method that performs sample classification from gene expression data, via "nearest shrunken centroid method". Centroids are the average gene expression for each gene in each class divided by the within-class standard deviation for that gene.
A disease response classifier using 23 genes was created to accurately predict response to alefacept (12.3% error rate). While the genes in this classifier should be considered as a group, some of the individual genes are of great interest, for example, cAMP response element modulator (CREM), v-MAF avian musculoaponeurotic fibrosarcoma oncogene family (MAFF), chloride intracellular channel protein 1 (CLIC1, also called NCC27), NLR family, pyrin domain-containing 1 (NLRP1), and CCL5 (chemokine, cc motif, ligand 5, also called regulated upon activation, normally T expressed, and presumably secreted/RANTES).
Although this study is small, and based on analysis of existing microarray data, we demonstrate that a treatment response classifier for alefacept can be created using gene expression of PBMCs in psoriasis. This preliminary study may provide a useful tool to predict response of psoriatic patients to alefacept.
Developing biomarkers that predict response to therapy is an ambitious goal of modern medicine. This is an aspect of personalized medicine that could transform our ability to treat patients successfully with a particular therapy in a cost-effective manner. Alefacept, an anti-CD2 fusion protein (Amevive, Astellas Pharma), is a biologic agent that often induces a remarkably durable remission . However, it produces a PASI 75 response (Psoriasis Area and Severity Index [PASI] response of greater than 75% improvement from baseline) in only approximately 30-50% of patients. Thus alefacept is an excellent example of a treatment that would benefit from being able to predict which patients with psoriasis would respond to this agent, and which patients might not respond.
The results of our original mechanism of action study of alefacept have already been published [2, 3]. In brief, patients were classified as histologic responders or non-responders, as described in the Methods section. Patients that responded to alefacept showed reductions in tissue gene expression of IFNγ, signal transducer and activator of transcription 1 (STAT-1), monokine induced by IFNγ (MIG), inducible NO synthase (iNOS), IL-8, and IL-23, as well as myeloid DCs (measured by immunohistochemistry for CD11c+ and CD83+ cells). As alefacept bound primarily to T cells and not DCs, we suggested that T cells were the primary target for therapy, but that DCs and a spectrum of type 1 inflammatory genes were coordinately suppressed. Furthermore, we demonstrated by FACS of PBMCs that in all patients, alefacept treatment caused a preferential decrease in effector memory T cells (CCR7- CD45RA-) for both CD4+ and CD8+ T effector memory cells. In contrast, central memory T cells (CCR7+CD45RA-) were less affected, and naïve T cells (CCR7+CD45RA+) were relatively spared. Circulating CD8+ effector T cells and Type 1 T cells (IFN-γ-producing) were also significantly reduced [2, 3].
The primary mechanism of action of alefacept is considered to be by killing CD2+ T cells by a cytotoxic mechanism (involving NK cell bridging), or by blocking CD2 signaling [4, 5]. In a previous study , our group established a new therapeutic mechanism for alefacept in psoriasis, as it also serves as an agonist for CD2 and induces positive T cell signaling responses. In this study, we analyzed genomic expression of circulating PBMCs, comparing baseline versus 24 hour time-point. During the first day of treatment in PBMCs, there was suppression of inflammatory genes, but perhaps surprisingly, a marked induction of mRNAs for STAT1, IL-8, and MIG. These agonistic effects of alefacept in PBMC were confirmed in vitro. These data demonstrated that alefacept activates gene expression in leukocytes and suggested that its therapeutic action may be as a mixed agonist/antagonist.
These findings suggested that differential activation of genes may categorize clinical responders to alefacept, and gave the first indication of differences in the pre-treatment circulating leukocytes in responders and non-responders. Thus these results led us to ask whether baseline gene expression in PBMCs might be used to classify responders versus non-responders and predict a priori who would respond to alefacept. This would have a dual benefit, allowing those responders to receive treatment with confidence, and sparing those who would not respond the cost, potential serious immunosuppressive effects and inconvenience of a course of therapy. The aim of this study was to mine our existing genomic data using alternative, previously developed analytic methods to generate a "genomic classifier" , a set of genes that could specifically predict response to alefacept. This "genomic classifier" could then be tested in a prospective clinical trial of alefacept in psoriasis.
Genomic expression profiles have been successfully used for disease classification and to predict response to treatment. In a seminal paper in 1999, Golub et al demonstrated that the type of haematological malignancy could be determined by class prediction using microarray data . Since then, other investigators have shown that genomic patterns of expression could be used to predict the progression and prognosis of cancer . Gene expression profiling of neoplastic tissue has been performed to develop a genomic classifier for response to a chemotherapy regimen for patients with advance colorectal cancer , or doxorubicin sensitivity in gastric cancers . Genomic classifiers have also been developed in breast cancer to predict tamoxifen-resistance , and docetaxel response . In chronic inflammation such as rheumatoid arthritis, response to etanercept (Enbrel, TNF-inhibitor) could be predicted by a genomic classifier consisting of specific combinations of gene doublets and triplets .
An IRB-approved clinical trial was conducted at Rockefeller University in 2002-2003, treating 22 patients with moderate-to-severe psoriasis with alefacept (7.5-mg weekly i.v. ×12 weeks). The initial aim of the clinical trial was to conduct a mechanism of action study, and the study was powered to produce groups of at least six patients that could be designated as responders versus non-responders (as defined below) to alefacept. Patients were recruited from local dermatologists, and by IRB-approved radio and print advertisements. 19 males and 3 females, (ages 29-68 years, median 49 years) were enrolled. Major inclusion criteria were: involvement of psoriasis vulgaris of >10% body surface area, no systemic treatment for at least 4 weeks before entering the study, no significant infections or immunosuppression, and no significant renal, hepatic, or other medical disease. Informed consent was obtained. The results of tissue analysis and peripheral blood analysis describing the mechanism of action of this biologic agent have already been published [2, 3], and are discussed in the Background section.
Processing of specimens for microarray
Initial microarray data from PBMCs of these patients has been published . Briefly, peripheral blood draws were taken before alefacept administration. PBMCs were isolated and stored at -80°C, until required. Pre-treatment RNA was extracted, and hybridized to HGU95Av2 Affymetrix Gene Chip containing probe sets representing 12,000 genes, using standard methods.
Quality Control, Pre-processing and Filtering
Gene Chip CEL files were scrutinized for spatial artefacts using Harshlight package https://mustat.rockefeller.edu/harshlight. Intensity values (CEL files) were pre-processed to obtained expression values using GCRMA algorithm. Expression values were filtered to eliminate probe sets with low variation or low intensity. Probe sets with standard deviation greater than 0.3, and expression values greater than 3 in at least 1 sample, were kept for further analysis, leaving a total of 5218 probe sets. Genes were annotated using up-to date annotation from of HGU95av2 chips available at Bioconductor. The data discussed in this publication have been deposited in NCBI's Gene Expression Omnibus and are accessible through GEO Series accession number (GSE18948).
We used a discriminant analysis method that performs sample classification from gene expression data, via "nearest shrunken centroid method" . This method is a modification of the conventional nearest centroid method , where centroids for each gene (average gene expression for the gene in each class) are divided by the within-class standard deviation in order to give more weight to genes with smaller variations across samples in the same class. Then, for prediction, every new sample is classified based on the gene expression profile of the sample by the following prediction rule: The class whose centroid is closest (by euclidean distance) to the gene expression profile of the sample is the predicted class for that new sample.
Nearest shrunken centroid classification makes one important modification to conventional nearest centroid classification. It "shrinks" each of the class centroids toward the overall centroid for all classes by an amount called the "threshold". This shrinkage consists of moving the centroid towards zero by threshold, setting it equal to zero if it hits zero: i.e if threshold = 2, a centroid of 3.2 would be shrunk to 1.2 and a centroid of 1.2 would be shrunk to zero. After shrinking the centroids, the new sample is classified by the prediction rule of the nearest centroid method (see above), but using the shrunken class centroids. This method has two advantages: it can make the classifier more accurate by reducing the effect of noisy genes, and it performs automatic gene selection. If a gene is shrunk to zero for all classes, then it is eliminated from the classifier. Alternatively, it may be set to zero for all classes except one, indicating that high or low expression for that gene characterizes that class.
Results and Discussion
Demographic details and PASI scores for patients used to develop genomic classifier to alefacept.
PASI End of treatment
Microarray data on 9 responders and 7 non-responders were available for further analysis using the discriminant analysis method. Figure 2 shows the misclassification error rate (Figure 2A) and the false discovery rate (Figure 2B) for thresholds ranging from 0-3. A threshold of 2.25 was chosen to create the final predictor (red arrow), as it rendered the best performance of the classifier in the cross-validation stage. The error rate for this final predictor was 0.123 (12.3%), as two non-responder patients were incorrectly classified as responders (patients 6 and 7, Figure 2C). However, the classifier correctly identified all responders as responders (patients 8-16). Classifying a responder as a non-responder would be the most costly error in terms of patient treatment, because otherwise a potential responder patient would be incorrectly left without treatment. However, this is still an improvement over the current situation as clinicians try to decide which therapeutic agent is best for a given patient. Approximately four out of ten patients would respond to alefacept (given a 30-50% therapeutic response rate); if this predictor is validated with the same error rate (12.3%), approximately five out of six patients would respond to alefacept. The false discovery rate for this final predictor was smaller than 0.1 (Figure 2B).
Genes that act as a genomic classifier for response to treatment of psoriasis with Alefacept.
cAMP responsive element modulator
v-maf musculoaponeurotic fibrosarcoma oncogene homolog F (avian)
chloride intracellular channel 1
SAM and SH3 domain containing 3
WEE1 homolog (S. pombe)
amine oxidase (flavin containing) domain 2
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 3
proteasome (prosome, macropain) subunit, beta type, 3
phospholipase C, beta 1 (phosphoinositide-specific)
sulfotransferase family, cytosolic, 1A, phenol-preferring, member 1
NLR family, pyrin domain containing 1
ATP synthase, H+ transporting, mitochondrial F1 complex, O subunit (oligomycin sensitivity conferring protein)
POU class 2 homeobox 2
ferritin, light polypeptide
chemokine (C-C motif) ligand 5
neuroblastoma breakpoint family, member 10
peptidylprolyl isomerase B (cyclophilin B)
purine-rich element binding protein A
interferon-induced protein 35
Tu translation elongation factor, mitochondrial
eukaryotic translation elongation factor 1 gamma
histone deacetylase 3
It is important to acknowledge the limitations of our study. The data-base for this study was small, as we were restricted to the clinical trial sample size, and the number of patients with good quality RNA and chip data. Although this data has been previously analyzed to find genes that were differentially expressed between responders and non-responders, this time we asked a different question of the data, specifically, could genes expressed in PBMCs before treatment predict response to alefacept. While we note that two of the non-responding patients were misclassified as responders, our preliminary conclusions suggest that this is a promising approach.
The genes in this classifier should be considered as a group. However some of the individual genes are of great interest. For example, cAMP response element modulator (CREM) is a gene that is highly increased in responders compared to non-responders, and this encodes activators and antagonists of camp-inducible transcription by differential splicing . In systemic lupus erythematosis, phosphorylated CREM correlated with decreased production of IL-2 and anergy in T cells . The pattern of expression of v-MAF avian musculoaponeurotic fibrosarcoma oncogene family (MAFF) is similar to CREF. This protein interacts with the upstream promoter region of the oxytocin receptor gene, and may be involved in the cellular stress response . Chloride intracellular channel protein 1 (CLIC1, also called NCC27) has the opposite expression pattern with an increase in non-responders, and a decrease in responders. Although the role of this gene in inflammation is not entirely clear, this gene does function as a nuclear chloride channel protein.
NLR family, pyrin domain-containing 1 (NLRP1) is involved in activation of caspase-1 and caspase-5 as part of the NALP1 inflammasome complex. The formation of this complex is important in the processing and release of bioactive IL-1β and IL-18 . NLRP1 is also involved in apoptosis. CCL5 (chemokine, cc motif, ligand 5, also called regulated upon activation, normally T expressed, and presumably secreted/RANTES) is a chemo-attractant for circulating monocytes, memory T helper cells, and eosinophils . Thus there were several interesting genes in this list, although the list should be taken as a whole for its use as a genomic classifier.
We conducted an alternative analysis of our previously published baseline peripheral blood microarray data , in order to determine the genes that would predict response to alefacept. We used a discriminant analysis method that performs sample classification from gene expression data . The database for this study was small, limited by the sample size of the clinical trial, and makes our conclusions preliminary. This approach and data are presented to show how pre-treatment peripheral blood microarray data can be used to identify a novel set of genes and develop a "genomic classifier". This genomic classifier could predict response to treatment and thus help physicians in selecting psoriasis patients who could benefit from treatment with Alefacept. This genomic classifier now needs to be tested prospectively.
Abbreviations used in this article are
Psoriasis Area and Severity Index
Peripheral blood mononuclear cells
False discovery rate
cAMP response element modulator
Avian musculoaponeurotic fibrosarcoma oncogene family
Chloride intracellular channel protein 1
NLR family, pyrin domain-containing 1
Chemokine, CC motif, ligand 5
monokine induced by IFNγ
signal transducer and activator of transcription 1
inducible NO synthase.
Research was supported by NIH grant UL1 RR024143. MSF is partially supported by NIH grant UL1 RR024143 from the National Center for Research Resources (NCRR). KRS and MSF are supported by the Milstein Program in Medical Research. MAL is supported by 1 K23 AR052404-01A1, and the Doris Duke Charitable Foundation. Partial support for the original study came from an unrestricted grant from Biogen.
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