- Open Access
Shipping blood to a central laboratory in multicenter clinical trials: effect of ambient temperature on specimen temperature, and effects of temperature on mononuclear cell yield, viability and immunologic function
© Olson et al; licensee BioMed Central Ltd. 2011
Received: 26 October 2010
Accepted: 8 March 2011
Published: 8 March 2011
Clinical trials of immunologic therapies provide opportunities to study the cellular and molecular effects of those therapies and may permit identification of biomarkers of response. When the trials are performed at multiple centers, transport and storage of clinical specimens become important variables that may affect lymphocyte viability and function in blood and tissue specimens. The effect of temperature during storage and shipment of peripheral blood on subsequent processing, recovery, and function of lymphocytes is understudied and represents the focus of this study.
Peripheral blood samples (n = 285) from patients enrolled in 2 clinical trials of a melanoma vaccine were shipped from clinical centers 250 or 1100 miles to a central laboratory at the sponsoring institution. The yield of peripheral blood mononuclear cells (PBMC) collected before and after cryostorage was correlated with temperatures encountered during shipment. Also, to simulate shipping of whole blood, heparinized blood from healthy donors was collected and stored at 15°C, 22°C, 30°C, or 40°C, for varied intervals before isolation of PBMC. Specimen integrity was assessed by measures of yield, recovery, viability, and function of isolated lymphocytes. Several packaging systems were also evaluated during simulated shipping for the ability to maintain the internal temperature in adverse temperatures over time.
Blood specimen containers experienced temperatures during shipment ranging from -1 to 35°C. Exposure to temperatures above room temperature (22°C) resulted in greater yields of PBMC. Reduced cell recovery following cryo-preservation as well as decreased viability and immune function were observed in specimens exposed to 15°C or 40°C for greater than 8 hours when compared to storage at 22°C. There was a trend toward improved preservation of blood specimen integrity stored at 30°C prior to processing for all time points tested. Internal temperatures of blood shipping containers were maintained longer in an acceptable range when warm packs were included.
Blood packages shipped overnight by commercial carrier may encounter extreme seasonal temperatures. Therefore, considerations in the design of shipping containers should include protecting against extreme ambient temperature deviations and maintaining specimen temperature above 22°C or preferably near 30°C.
Cell-based immunological assays are integral to monitoring the effects of immunotherapy clinical trials. The main clinical specimen obtained for these assays is whole blood collected in heparinized vacutainer tubes from which peripheral blood mononuclear cells (PBMC) are isolated. Assays of cellular immune responses to immune therapy depend on functional and viable PBMC. It is critical that outside factors, other than study parameters, do not introduce significant variability in the immune assays due to compromised PBMC integrity. Therefore, trials utilizing multiple clinical centers present challenges in how to best process and transport whole blood and tissue samples.
The need for specific guidelines for the shipment of biological specimens is of great concern for the conduct of multi-center clinical trails at the national and international level [1–3]. Both complex processing and delay before processing by individual laboratories increase the variability in specimen performance . In contrast, central laboratory processing lessens the variability introduced by multiple processing protocols but is more costly and may not be available for all investigators. It therefore becomes a critical issue in the design of multi-center clinical trials to determine whether biological specimens should be processed immediately, the same day, or after shipment to a central laboratory.
Early studies have demonstrated how time and temperature of storage affect lymphocyte viability and phenotype when whole blood is stored overnight at 4°C [5–7]. Storage at room temperature prior to processing also affects viability and blastogenic responses  as well as lymphocyte separation by Ficoll density centrifugation [9, 10]. The importance of establishing standard shipping parameters has been stressed in the infectious disease setting, in which a profound impact of shipping was noted on the lymphoproliferative responses to microbial antigens in both HIV-infected and healthy donors [11, 12]. Single cell-based techniques such as ELIspot assays [13–15], intracellular cytokine staining [16–19], and HLA-specific multimeric assays [20–22] are widely used and depend on optimal conditions for specimen handling in order to detect rare populations of peptide specific lymphocytes in response to immunotherapy. Several studies have confirmed that cryopreserved PBMC can be used reliably in these assays [23–26]. Use of cryopreserved samples, however, depends on optimal sample handling before and after cryopreservation. Some studies have defined optimal time intervals between venipuncture and cryopreservation [26–29] and optimal conditions for freezing . Also, handling and storage of cryopreserved PBMC have been evaluated, showing that fluctuations in sub-zero freezing temperatures can alter the viability and function of recovered lymphocytes; shipping conditions for frozen samples have also been addressed [31, 32]. However, the effect of ambient temperature changes during shipping or storage prior to cryopreservation has not been addressed.
It has been suggested that an interval of whole blood storage exceeding 8 hours (h) causes a significant decrease in cellular immune function . This finding provides rationale for immediate isolation and cryopreservation of PBMC at each participating clinical center and indeed, optimization of cryopreservation media and of thawing practices has improved recovery of immunological responses at the single cell level [25, 30]. However, processing of blood and cryopreservation of PBMC at off-site locations is expensive and requires oversight and quality control of the processing lab at each center. Thus, for many multicenter clinical trials of cancer vaccines and other therapies, all off-site whole blood specimens are shipped to a central laboratory according to a standard operating protocol, and monitored strictly for quality control and quality assurance. Our concern that shipping whole blood in different seasons, in various climates, may impact PBMC viability and function prompted this study. Specifically, we have addressed the effect of shipping temperatures on cell viability, recovery and function, and have modeled these in vitro when controlling for temperature.
Blood collection, processing and storage
Patients' blood specimens were derived from participants enrolled in one of three studies. Participants were enrolled in the clinical studies following informed consent, and with Institutional Review Board for Health Sciences Research approval (IRB-HSR# 10598, 10524, and11491) and review by the FDA (BB-IND# 9847 and 12191). Patients' blood specimens from 2 clinical trials (HSR# 1524(HSR# 10524 and 11491) were monitored during a 9 month period from late summer, through fall, winter and early spring. Two hundred and eighty-five blood specimens collected at participating clinical trial centers in Houston, TX and Philadelphia PA, were shipped to Charlottesville VA. Clinical laboratory analyses, including complete blood counts (CBC) and differential hematological counts, were performed at the individual centers and the results incorporated into a trial database. An additional 60 ml of blood were collected in 10cc heparinized vacutainer tubes (BDBiosciences, Franklin Lakes, NJ) and were shipped, in insulated packaging, by overnight courier at ambient temperature to the Biorepository and Tissue Research Facility (BTRF) at the University of Virginia (UVa) for processing and cryo-preservation, on the day they arrived, for future immunological testing in cell-based assays. Shipments of patients' blood specimens were continuously monitored using the TempCheck Sensor (Marathon Products, Inc., San Leandro, CA) to determine the temperature range to which blood samples were exposed when shipped overnight by commercial carrier, and to evaluate the effects of those temperatures on cell yield. Temperature gauges recorded the maximum and minimum temperatures attained inside the packages during shipment. Blood drawn at UVa was processed either the same day or the following day, depending on when in the day it was drawn. The volume of blood collected, and the number of viable PBMC isolated were recorded by the BTRF. These values were used to determine the cell yield before cryo-preservation. In all cases, the PBMC fraction of whole blood was collected from Leucosep™ (Greiner Bio-One, Monroe, NC) tubes following centrifugation for 10 minutes at 1000 × g.
The expected cell yield for each sample was calculated from the CBC and differential tests performed on whole blood at the originating clinical laboratory. The absolute lymphocyte and absolute monocyte counts calculated from the CBC and differential were combined and multiplied by the volume of blood collected to represent the expected total PBMC in the blood (expected cell yield). Additional File 1 provides a table of cell count data from each center. The table shows the calculated percentage (mean, median, and quartiles) of lymphocytes and monocytes derived from differential and complete cell counts. The number of PBMC isolated by Ficoll separation, divided by the expected cell yield provides the ratio cell yield. Ratio cell yields of less than 1 are expected due to losses in Ficoll separation. However, because the Ficoll separations were done by the same central laboratory and according to a consistent protocol, differences in ratio cell yields in different subgroups of specimens are primarily attributed to effects of shipping conditions.
Incubation conditions for whole blood
In one set of experiments, approximately 7-8 ml whole blood were collected into each of eleven heparinized vacutainer tubes from six healthy donors according to IRB protocol 10598 and were labelled to define the temperature conditions to which they would be exposed. Each tube was incubated at various temperatures over a 24 h period at conditions intended to model what may happen in overnight shipping conditions (Additional File 2). After a 1-2 h equilibration period at room temperature (RT, 22°C), tubes from each sample were placed in each of the 4 conditions: (a) temperature-controlled refrigerated centrifuge set at 15°C, (b) 22°C as a control condition, (c) water bath set at 30°C, or (d) water bath set at 40°C. In addition, one tube was placed in a 50°C water bath for 2 h, but this condition invariably led to hemolysis and the samples were not evaluable. For each temperature condition (other than RT), one tube was exposed to that low or high temperature for 2, 8 or 12 h, and then each was returned to RT for the remaining 24 h study period. Thus, one tube served as an untreated control and was at kept at RT for the whole 24 h. After these incubations, PBMC were isolated from each blood sample by Ficoll density gradient as described above. Viable cell numbers were determined by trypan dye exclusion. PBMC were cryopreseved in freezing medium (90% FCS, 10% DMSO) overnight at -80°C, then transferred to vapor phase liquid nitrogen for 1-4 weeks before thawing for analysis.
Cells producing IFNγ after antigen specific and non-specific stimulation were enumerated by ELIspot assay as described previously [33, 34]. In brief, PBMC were thawed in pre-warmed RPMI1640 (Invitrogen, Carlsbad CA) containing 10% human AB serum (HuAB; Gemini) and 100 Units/mL of DNase I (Worthington Biochemical Corp., Lakewood, NJ). Cells were centrifuged at 350 × g and adjusted to the desired cell density in RPMI 1640 supplemented with 10% HuAB serum and plated into PVDF-membrane plates coated with anti-interferon gamma antibody (Pierce-Endogen, Thermo Scientific, Rockford IL). Phytohemagglutinin (PHA), phorbol myristate acetate (PMA and ionomycin were obtained from Sigma-Aldrich (St. Louis, MO). A pool of 35 MHC Class I restricted peptides consisting of peptides from cytomegalovirus, Epstein-Barr and influenza virus proteins (CEF peptide pool; ; Anaspec, Fremont CA) or media alone were added in quadruplicate and cultures incubated overnight at 37°C in a 5% CO2 atmosphere. Spots were developed according to standard protocol and enumerated on a BioReader 4000 (Bio-Sys, Karben, Germany) plate reader.
CD3, CD4, CD8 and CD56 positive lymphocyte populations were enumerated by flow cytometry using fluorescent-labelled antibodies (BDBiosciences, San Diego, CA). Cells were washed, suspended in PBS (Invitrogen) containing 0.1% BSA (Sigma) and 0.1% sodium azide (Sigma). Titrated amounts of each reagent were added to cells, incubated, washed free of excess stain, and fixed in paraformaldehyde. To determine whether there was an increase in apoptosis due to different storage conditions, thawed PBMC were incubated overnight at 37°C in 5% CO2 in RPMI 1640 + 10% Human AB serum. The next day, PBMC were surface stained with fluorescently labeled antibodies to CD3, CD4, and CD8, then stained with Annexin V according to manufacturer's instructions (BDBioscience, San Diego, CA) and 7-AAD (EMD Chemicals, Inc., Gibbstown, NJ) to determine the level of apoptosis [36–38]. Cells were acquired on a FACSCalibur flow cytometer maintained by the Flow Cytometry core facility of the University of Virginia. Data were analyzed with FlowJo software (Treestar, Ashland OR).
Testing of Blood Shipping Packages
The standard shipping container used in our clinical trials was obtained from Safeguard Technologies Corp. (Conshohocken, PA). It consisted of a white corrugated box fitted with a hydrophilic foam-lined clear plastic snap-lock case inserted into a plastic zip lock bag. This was placed inside a cardboard shipping container lined with 1" thick Styrofoam. An alternate packaging design was provided by JVI (Charlottesville VA) and consisted of a 14" × 11" × 5" box of 200# corrugated cardboard insulated with Control Temp Packaging foam of 1" thickness. Inside was placed a 12" × 9" × 3" clamshell type clear plastic box containing an 11" × 8.5" × 5/8" foam vial holder.
Each type of shipping container was tested for its ability to maintain temperature in cold ambient conditions (e.g.: during winter months). Forty heparinized vacutainers were filled with water and equilibrated to 37°C. Ten vacutainers were placed inside each of 4 packages (2 of each type). Each package type received a gel pack conditioned at either 37°C or 22°C which was then placed alongside the vacutainer holder. One probe of an indoor/outdoor thermometer (Taylor Precision Products, Oak Brook IL) was placed inside the package while another remained outside to monitor external ambient temperature. Packages were placed either in a cold room at 4°C for a minimum of 12 h or were handled in a manner to model the experience of a package being shipped via motor vehicle overnight in a non-heated compartment. Temperatures were recorded every 15 minutes during the first hour, and 30-60 minutes thereafter.
Additional testing of the JVI packaging material was performed by R.N.C. Industries Inc. (Norcross GA 30071) at high external package temperature. The clamshell foam holder containing vials of liquid was placed inside the package. Two 12 oz Control Temp gel packs conditioned at 20°C were placed in the clamshell onto which the foam vial holder (including the 1/4" foam above and below) containing five 5/8" vials filled with water conditioned at 20°C was placed inside. The package was closed, put at 45°C and the internal package temperature was monitored for 48 hours using an Omega OMB-DAQ-55 USB data acquisition system, serial number #156772. T thermocouples were calibrated 2 months earlier using a stirred water bath calibration.
The MIXED procedure in SAS 9.1.3 (SAS Institute, Cary, NC) was used to analyze the effects of temperature (3 levels) and duration (3 levels) on outcomes including ELIspot, phenotype, and viability. These effects were modeled jointly (main effects plus interactions) for each outcome measure and outcome measurements were first normalized by division of the raw data by the donor value at RT for 24 h. Since donors served as blocks and contributed an observation from each condition (i.e. each combination of temperature and duration level), intra-donor correlation was modeled assuming a compound symmetry structure in the residual covariance matrix. Degrees of freedom were calculated using the Kenward-Roger method. To assess the effects of storage under different temperature conditions on apoptosis among CD4 and CD8 populations, a modeling scheme similar to the one above was performed using calculated logits as the outcome measure. This is defined as the loge([pi/1-pi]/[pc/1-pc]) where p = the proportion of cells that are apoptotic or necrotic (as defined by Annexin V and 7AAD staining); i = the storage conditions of the whole blood specimen; and c = the storage condition of the control specimen at RT for 24 hours. All tests were assessed at α = 0.05.
Effect of shipping temperatures and extreme changes in temperature on the cell yield for clinical trial specimens
Effect of temperature on cell yield before cryopreservation
Effect of exposure to different incubation conditions on PBMC isolation from whole blood and recovery after cryo-preservation
Cell Yield before Cryopreservation
Cell Recovery after Thawing
0.85 (0.60, 1.10) p = 0.22
0.88 (0.63, 1.13) p = 0.32
0.59 (0.34, 0.84) p = 0.003
1.00 (0.70, 1.30) p = 0.99
1.02 (0.72, 1.32) p = 0.88
0.66 (0.36, 0.97) p = 0.031
0.90 (0.65, 1.15) p = 0.40
1.02 (0.76, 1.27) p = 0.90
1.00 (0.75, 1.25) p = 1
1.12 (0.82, 1.42) p = 0.41
1.20 (0.90, 1.50) p = 0.19
1.19 (0.88, 1.49) p = 0.21
0.87 (0.62, 1.12) p = 0.30
0.83 (0.58, 1.08) p = 0.16
0.79 (0.53, 1.06) p = 0.12
0.91 (0.61, 1.22) p = 0.56
0.78 (0.48, 1.08) p = 0.14
0.63 (0.32, 0.95) p = 0.026
Effect of Temperature on Cell Recovery after cryopreservation
We hypothesized that shipping temperatures may impact cell recovery and viability after storage in liquid nitrogen. The total number of viable cells (trypan blue dye exclusion) was recorded for each of the PBMC samples exposed to varied temperatures as reported above. Percent recovery was calculated as the ratio of recovered viable cells to the number of viable cells initially frozen. Each condition was compared to storage at RT for 24 h. Significant reduction of PBMC recovery was associated with storage of blood 12 h at 15°C or 40°C but not with either 2 h or 8 h (Table 1). However, at 30°C, the trend favored higher recoveries of PBMC, at all time points, than that seen at RT.
Effect of temperature on viability and phenotype after cryo-storage
These samples were also assessed by flow cytometry for evaluable PBMC populations and the selective loss of T lymphocyte sub-populations after cryo-preservation. Changes in the PBMC population were not reflected in the proportion of CD4+ and CD8+ lymphocyte sub-populations (Additional file 3) or in the proportion of CD56+ lymphocytes (data not shown) compared to that seen when whole blood is stored overnight at RT.
Effect of temperature on cell function after cryostorage
Package testing in high and low ambient temperatures
Pre-warmed gel packs extend the time above 15°C when shipping at cold temperatures
Gel Pack Temperature
Recently much-needed attention has been given to the conditions under which blood specimens, collected for correlative studies of immune therapy, are handled prior to PBMC isolation. How samples are processed and shipped from trial sites as whole blood or separated PBMC can affect the outcome of immunological monitoring of vaccine-based immunotherapeutic clinical trials. Arguably, it is optimal to assay a blood sample immediately and at the site where it is collected, as is done for most routine clinical laboratory tests. However, for novel or experimental correlative studies, this is not usually feasible, since expertise for those tests requires specialized laboratories. Also, an argument can be made for evaluating pre- and post-treatment blood samples in the same assay to provide internal controls. Thus, blood samples often are shipped to centralized laboratories for correlative studies where they are often cryopreserved for later batch analysis. Another question is whether cryopreservation should be done at each site, or whether whole blood should be shipped to the central lab for processing there. Several details of cryopreservation methods can impact PBMC function and viability ; so if cell isolation and cryopreservation is done at each site, there needs to be intensive training and quality assurance to confirm comparable methods and results. Though it is an option, this approach often is infeasible for financial and organizational reasons. Thus, it is common for whole blood to be shipped from multiple sites to a central laboratory for PBMC isolation and cryopreservation, for later analysis. However, the possible impact of temperature during shipping, and prior to processing, has not been systematically addressed. In this study, we have focused on the effect of temperature during shipping to assess its variation based on season of the year, and to assess the impact of temperature on PBMC viability and function.
In multiple studies in the HIV literature, delayed processing of whole blood has been identified as a major factor affecting PBMC performance in cell-based immunological assays [26–29]. Delay in processing during overnight shipping (at least 24 h) decreased responses to microbial antigens in lymphoproliferative assays  indicating the need for defined transportation conditions for specific antigens. However, that study did not assess the impact of temperature during shipping. The same investigators also demonstrated that the way in which frozen PBMC are thawed, and how long PBMC are cryopreserved, will impact lymphoproliferative responses to specific antigens . Bull et al. found that the time from phlebotomy to crypreservation should be less than 8 hours for optimal performance in cell based assays such as ELIspot and intracellular cytokine staining assays . Delaying processing of whole blood by 6 hours also impaired the response of antigen-presenting cells to Toll-like receptor ligands . On the other hand, Whiteside et al. showed the phenotype and function of dendritic cell populations derived from apheresis products shipped overnight were not markedly different from DC generated from cells immediately frozen after elutriation. Smith et al. showed that delayed processing of blood resulted in a decrease in cell viability as well as a marked reduction in IFNγ SFC in response to varicella zoster antigen ; the presence of DNase partially restored the response . Kierstead et al. demonstrated that cryopreservation of PBMC should be done within 12 hours of phlebotomy. However, in these two prior studies, the whole blood  or PBMC  was stored or shipped at 4°C overnight before cryopreservation. It is not known whether there were negative effects from storing or shipping at 4°C. Our data show that there is better viability, cell yield, and function when cells are shipped at room temperature (22°C) or 30°C than at 15°C, and it is generally accepted that storage of whole blood at 4°C negatively impacts cell viability , function , and population recovery [6, 7, 43, 44]. Acknowledging the range of data in the literature, in a separate study, we are also evaluating the function of PBMC processed the same day (< 8 h) or after overnight shipping or storage (manuscript in preparation). However the current manuscript focuses on the impact of temperature during shipping in those cases when overnight shipping is necessary.
In some prior studies, statistical differences between immediate and delayed processing of specimens were influenced not only by the delay in processing but also by the method of processing and by the type of anticoagulant used . Thus, although there was a statistical decrease in viability and recovery when whole blood was collected in heparin and isolated by Accuspin technology (centrifuge tube divided into two chambers by means of a porous high-density polyethylene barrier, known as a frit), no significant decrease was evident when PBMC were collected at the interface of plasma and Ficoll. Similarly, significant differences in viability (but not recovery) between fresh and delayed samples were evident when collected in ACD or EDTA anticoagulants but not in heparin when PBMC were isolated directly onto a Ficoll cushion. Furthermore, the functionality of PBMC was not significantly impaired by either method when measured in an IFNγ-ELIspot assay in response to the CEF pool of peptides.
The observations leading to the present study come from the multi-center clinical trials we have conducted at the University of Virginia in collaboration with Cancer centers in Houston TX and Philadelphia PA. Blood specimens shipped from these locations encounter extreme seasonal climate conditions. On the other hand, blood specimens at the on-site location are, for the most part, collected, stored and processed with no exposure to extreme temperatures and processed either on the same day or after storage overnight at room temperature. This study has addressed 1) the seasonal changes in temperature inside packages of blood specimens during shipping in the U.S., 2) changes in temperature inside packages simulating hot or cold ambient temperatures during shipping, and 3) the effects of temperatures above and below room temperature on PBMC numbers, viability, and function. These studies are relevant to shipping blood specimens for correlative studies in many settings.
We are not aware of prior work tracking temperature ranges encountered within blood shipping containers or their variation by season of the year. We found that shipping of blood in insulated containers by contracted overnight carriers is associated with large seasonal variations in temperature inside the packaging, ranging from -1°C in winter to 35°C in summer, with most in the range of 4°-32°C. Thus, blood samples in transit are frequently exposed to high temperatures at or above 30°C and low temperatures that approach or go below freezing temperatures at least transiently. The monitoring devices used in these shipments recorded the minimum and maximum temperatures but not the duration of each temperature. Thus, we also studied the changes over time in a dynamic manner in hot or cold conditions designed to mimic changes that may occur during shipping, and found that insulation maintains internal temperature below 30°C for up to 21 hours in ambient temperatures that likely exceed those experienced during shipping (45°C). We found in very cold ambient conditions, that the insulated containers maintained the internal temperatures above 15°C for almost 6 hours and above 20°C for over 3 hours, with the aid of thermal packs pre-warmed at 37°C.
We have found that incubation of whole blood at 50°C caused unacceptably high loss of PBMC (data not shown). Storage at 15°C or 40°C for 12 h causes significant decreases in cell yields, viability and/or function but exposure to those temperatures for 2 hours, or in some cases even 8 hours is associated with PBMC yields, viability and function comparable to those found from blood stored at RT. The apoptosis rates in this study of about 30-35% in thawed cells incubated overnight are higher than observed in prior work where apoptosis was measured directly after thawing . It is not uncommon, however, that cells undergo a delayed-onset cell death (reviewed by Baust ) which may account for the increase in apoptosis measured here. Other studies also confirm that the total viability decreases after overnight incubation . Regardless, we find that there is function in the PBMC that are viable after overnight incubation. Incubation at 15 or 30°C is associated with comparable T cell function assessed by ELIspot assay to that seen with PBMC stored at RT. Interestingly, we found that incubation at 30°C for periods up to 12 h was even associated with equivalent or better yields, viability and function compared to samples left at RT. However, incubation at 15°C or 40°C for 8-12 h was associated with decreased viability and function. Colder temperature (15°C) primarily affected cell yield after Ficoll separation and reduced recovery following cryopreservation. Recovery may be due to a perturbation in cell density  or formation of cell aggregates [5, 45]. No increase in apoptosis relative to that seen when blood was stored at room temperature was noted at lower temperatures which is consistent with other data showing reduced apoptotic rate of PBMC held at 4°C for 24 hours .
Recommendations for shipping whole blood specimens
Time of Year
37°C warm packs
We propose that controlled and monitored shipping temperatures may mitigate negative effects of shipping blood in multicenter trials. Careful attention to the shipping containers and testing in ambient temperature is recommended. Certainly one way to prevent negative effects of cold or hot temperatures during shipping of blood specimens is to isolate PBMC or other cellular elements prior to shipping, and either to cryopreserve them or to assay them on site. This introduces other sources of error and substantial costs, by the need to maintain quality control assay validation across multiple laboratories, which is problematic. We believe there is a role for shipping blood specimens for centralized assays where those assays can be performed in batches with appropriate controls, but attention to details of shipping conditions are warranted in such circumstances, to maximize the reliability of the results. It also is appropriate, in multicenter trials, to stratify patients by institution to control for systematic variations in temperature during shipping that may be encountered depending on the latitude of the institution and the shipping distance.
Blood packages shipped overnight by commercial carrier may encounter extreme seasonal temperatures. Warmer temperatures favor greater cell yields of shipped blood specimens whereas colder temperatures for long periods of time lower cell recovery and viability. Temperatures ≥40C for ≥8 hours reduces cell viability and functionality after cryo-preservation. In the design of containers for blood shipment, maintaining an ambient temperature between 22°C and 30°C should be considered.
The authors express their gratitude for R.N.C. Industries Inc. Lab, 640 Langford Drive, Norcross GA 30071 in conducting the temperature performance test for the JVI Control Temp shipping container. This study was funded by NIH/NCI grants R01 CA118386 and R21 CA103528 (to C.L.S). Support was also provided by the University of Virginia Cancer Center Support Grant (NIH/NCI P30 CA44579: Clinical Trials Office, Biorepository and Tissue Research Facility, Flow Cytometry Core, and Biomolecular Core Facility); the UVA General Clinical Research Center (NIH M01 RR00847). Also, philanthropic support was provided from the Commonwealth Foundation for Cancer Research and Alice and Bill Goodwin. Additional philanthropic support was provided by Frank and Jane Batten, the James and Rebecca Craig Foundation, George S. Suddock, Richard and Sherry Sharp, and the Patients and Friends Research Fund of the University of Virginia Cancer Center. No corporate funding support was provided for this study.
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