Background
Highly active antiretroviral therapy (HAART) has significantly improved the morbidity and mortality of HIV-infected patients. A total of 37 licensed drugs are available for optimal antiretroviral combinations [
1]. However, not all patients can profit from long-term therapy, and patients may still have an increased risk of death from non-AIDS-associated malignancies. Most patients receiving HAART have some persistent immune dysfunction [
2]. Non-AIDS-associated malignancies are becoming a large burden on the healthcare system owing to the improved survival of HIV-infected patients receiving HAART.
Increasing evidence has demonstrated that drugs targeting multiple targets of HIV-1 infection usually have amplified therapeutic efficacy [
3].
Aikeqing (AKQ), composed of Radix
Aconiti Lateralis Preparata (
Fu Zi),
Herba Epimedii (
Yin Yang Huo), Rhizoma
Zingiberis (
Gan Jiang), Radix
Glycyrrhizae (
Gan Cao), Radix
Ginseng (
Ren Shen), Radix
Salviae Miltiorrhizae (
Dan Shen), Rhizoma
Polygoni Cuspidati (
Hu Zhang),
Poria (
Fu Ling), Cortex
Phellodendri (
Huang Bai), and Radix
Scutellariae (
Huang Qin), was designed based on the symptoms and characteristics of HIV/AIDS patients by investigators at the Institute of Tropical Medicine, Guangzhou University of Chinese Medicine [
4]. Pilot clinical studies [
4,
5] reported beneficial effects of AKQ in the treatment of HIV patients in China, by improving their quality of life and reducing side effects related to medications. However, the HIV loads and CD4
+ T cell counts, which are routinely measured to monitor HIV disease progression, were not determined in the treated patients because of the associated costs and technical constraints.
Rhesus macaques closely resemble humans in anatomy, physiology, drug metabolism, and other characteristics. Moreover, their susceptibility to SIV/SHIV infection makes them a superior animal model for testing of anti-HIV drugs. Chinese-origin rhesus macaques (Ch-RMs) are the most appropriate species for studying SIV/SHIV infection and AIDS pathogenesis [
6,
7]. To our knowledge, there are no reports on the use of SHIV-infected Ch-RMs to test the efficacy of a Chinese medicine.
This study aimed to determine the anti-HIV activity of AKQ in chronically SHIV89.6-infected Ch-RMs.
Methods
Herbal materials and AKQ extraction
AKQ was provided by the Tropical Medicine Institute, Guangzhou University of Chinese Medicine, and composed of Radix
Aconiti Lateralis Preparata,
Herba Epimedii, Rhizoma
Zingiberis, Radix
Glycyrrhizae, Radix
Ginseng, Radix
Salviae Miltiorrhizae, Rhizoma
Polygoni Cuspidati,
Poria, Cortex
Phellodendri, and Radix
Scutellariae at ratios of 10:5:5:5:3:3:3:3:1.5:1.5 (Table
1). All air-dried herbs in AKQ are regionally well-known herbal medicines that are commercially used in China, and were purchased from Guangzhou Medicine Company (Guangzhou, China). The authenticity was identified by herbalists within that company, and re-confirmed by Prof. Ying-Jie Hu through morphological and anatomical identifications. The voucher specimens (AKQ HM-1–AKQ HM-10) were deposited at the Tropical Medicine Institute, Guangzhou University of Chinese Medicine.
Table 1
Composition of Aikeqing
Fuzi | Radix AconitiLateralisPreparata | Aconitum carmichaeli Debx. | Black slice of root | 10 |
Yinyanghuo | Herba Epimedii | Epimedium brevicornum Maxim. | Overground portion | 5 |
Ganjiang | Rhizoma Zingiberis | Zingiber officinaleRosc. | Rhizoma | 5 |
Gancao | Radix Glycyrrhizae | Glycyrrhiza uralensis Fisch. | Root and Rhizoma | 5 |
Renshen | Radix Ginseng | Panax ginseng C. A. Mey. | Root | 3 |
Danshen | Radix SalviaeMiltiorrhizae | Salvia miltiorrhizaBge. | Root | 3 |
Huzhang | Rhizoma Polygoni Cuspidati | Polygonum cuspidatum Sieb. etZucc. | Root | 3 |
Fuling | Poria | Poriacocos (Schw.) Wolf. | Sclerotium | 3 |
Huangbai | Cortex Phellodendri | Phellodendron chinensis Schneid. | Bark | 1.5 |
Huangqin | Radix Scutellariae | Scutellaria baicalensis Georgi | Root | 1.5 |
The raw herbal materials were mixed and extracted in 20 volumes of boiling water for 2 h, with the extraction repeated three times. The aqueous extracts were filtered and the suspension was collected. The filtrate was added to 2 volumes of 95 % (v/v) ethanol. The two suspensions were mixed thoroughly and left to stand for 10 h. The second mixture was filtered and the suspension was collected. The extraction solution was concentrated by stove-drying the residue, smashed to a fine powder, and stored in a desiccator until use.
Animals and study design
The nine juvenile male Ch-RMs (age: 3–6 years; body weight: 5.5–10.2 kg) used in this study were colony-bred rhesus macaques (
Macaca mulatta) of Chinese origin that were maintained in accordance with the regulations of the American Association for Assessment and Accreditation of Laboratory Animal Care at the Kunming Primate Research Center, Kunming Institute of Zoology, Chinese Academy of Sciences. All experimental procedures were performed at the ABSL-3 Laboratory according to the guidelines approved by the Ethics Committee of Kunming Institute of Zoology (Approval Number: SWYX-2011020; Additional file
1). Room temperature of the ABSL-3 Laboratory was maintained at 20–28 °C, with a relative humidity of 35–60 % and a 12-h/12-h light/dark cycle. The Ch-RMs were housed in stainless-steel cages (800 × 1000 × 1000 mm), and fed a monkey diet as well as fresh fruits, vegetables, and nuts. All animals had free access to feed and water ad libitum. The general conditions of the Ch-RMs, such as health status, behavior, eating habits, and stools, were observed daily by a veterinarian. The animal studies were performed following the ARRIVE guideline (Additional file
2).
All animals were demonstrated to be seronegative for SIVmac, simian T cell leukemia virus type 1, simian retrovirus type 1 (type D retrovirus), and herpesvirus B. To allow for achievement of steady-state parameters, treatment was initiated at week 11 in the early phase of chronic infection and lasted for 8 weeks thereafter. Blood samples were obtained biweekly during the infection. One animal (#02067) in the control group died at the initiation of therapy (day 5), suggesting that its immune response might not have been sufficient for protection against SHIV infection. All data from week 12 onward refer to a total of two animals in the control group.
SHIV infection and treatment
The Ch-RMs were inoculated intravenously with 1000 TCID50 (50 % tissue culture infectious doses) of cell-free SHIV89.6 grown in CEM × 174 cells. The animals were arbitrarily divided into three groups according to the cage placement within rooms in the animal house: control group (water 1 mL/kg): #02067, #06003, #06025; AKQ high-dose group (AKQ 1.65 g/kg): #03057, #04331, #06403; and AKQ low-dose group (AKQ 0.55 g/kg): #01089, #05077, #06311. AKQ was administered to the Ch-RMs once-daily by the intragastric route through a nasogastric tube (Sofine, Zhejiang, China).
Plasma collection
For blood collections, the animals were immobilized with ketamine-HCl (10 mg/kg body weight) injected intramuscularly at the lateral thigh muscles. Peripheral blood (5 mL) was collected into vacutainer tubes (Zhiyuan, Wuhan, China) containing EDTA-K2 as an anticoagulant. Blood was collected from the lateral aspect of the hind limb. Plasma was separated by centrifugation of the blood in an Allegra X-12 centrifuge (Beckman Coulter, Fullerton, CA, USA) at 900×g for 10 min at 4 °C, and stored at −80 °C until further processing and analysis.
Hematological parameter assays
Aliquots of blood (100 μL) were transferred to tubes for hematological analyses. Hematological parameters were measured using an automated hematological analyzer machine (BC-2800Vet; Mindray, Shenzhen, China). The abbreviations and units of the hematologic parameters are described in Table
2.
Table 2
Hematological parameters of SHIV89.6-infected Ch-RMs during Aikeqing treatment
WBC | H | 7.2 ± 2.0 | 8.1 ± 0.8 | 7.2 ± 1.1 |
L | 7.0 ± 1.6 | 8.2 ± 0.4 | 8.4 ± 0.6 |
C | 7.6 ± 1.9 | 8.0 ± 2.0 | 7.3 ± 2.3 |
Mon (%) | H | 7.3 ± 0.7 | 8.1 ± 2.2 | 7.7 ± 2.1 |
L | 7.9 ± 0.9 | 8.9 ± 1.6 | 7.6 ± 0.9 |
C | 7.6 ± 1.1 | 8.1 ± 1.3 | 8.2 ± 0.3 |
Mon (109/L) | H | 0.4 ± 0.1 | 0.5 ± 0.1 | 0.4 ± 0.2 |
L | 0.4 ± 0.2 | 0.4 ± 0.4 | 0.4 ± 0.2 |
C | 0.6 ± 0.3 | 0.4 ± 0.3 | 0.7 ± 0.2 |
RDW (%) | H | 15.6 ± 0.3 | 16.4 ± 0.4 | 15.5 ± 0.1 |
L | 15.8 ± 0.3 | 16.1 ± 0.3 | 15.5 ± 0.8 |
C | 14.7 ± 0.6 | 16.2 ± 0.2 | 15.5 ± 1.0 |
RBC (1012/L) | H | 7.5 ± 0.4 | 6.6 ± 0.4 | 6.8 ± 0.1 |
L | 7.1 ± 0.4 | 5.6 ± 0.4 | 6.0 ± 0.6 |
C | 7.1 ± 0.3 | 6.0 ± 0.9 | 5.8 ± 0.8 |
HCT (%) | H | 58.7 ± 2.0 | 51.2 ± 3.4 | 53.9 ± 1.0 |
L | 53.2 ± 2.9 | 42.8 ± 3.2 | 46.7 ± 4.9 |
C | 52.9 ± 2.4 | 46.0 ± 7.2 | 45.6 ± 7.0 |
Lym (109/L) | H | 1.7 ± 0.3 | 2.0 ± 0.2 | 2.5 ± 0.5 |
L | 1.5 ± 0.2 | 1.6 ± 0.6 | 2.0 ± 0.3 |
C | 1.8 ± 0.5 | 1.8 ± 0.7 | 2.0 ± 0.3 |
Lym (%) | H | 22.4 ± 6.0 | 27.3 ± 10.5 | 36.9 ± 12.5 |
L | 19.0 ± 9.7 | 17.4 ± 5.9 | 34.0 ± 7.8 |
C | 22.8 ± 12.4 | 23.2 ± 22.0 | 32.7 ± 13.9 |
MCV (fL) | H | 74.6 ± 0.2 | 77.5 ± 0.5 | 79.0 ± 0.3 |
L | 75.0 ± 0.5 | 76.9 ± 0.4 | 78.6 ± 0.2 |
C | 74.3 ± 0.5 | 77.3 ± 0.8 | 78.5 ± 1.5 |
MCH (pg) | H | 24.4 ± 0.4 | 25.6 ± 0.6 | 26.8 ± 0.5 |
L | 23.9 ± 1.2 | 25.0 ± 0.3 | 26.2 ± 0.2 |
C | 22.9 ± 1.9 | 24.1 ± 1.9 | 24.2 ± 2.4 |
MCHC (g/L) | H | 328.3 ± 4.2 | 331.3 ± 7.8 | 339.3 ± 6.7 |
L | 319.3 ± 13.9 | 326.0 ± 4.4 | 333.3 ± 3.2 |
C | 309.0 ± 23.4 | 311.7 ± 22.0 | 308.3 ± 26.5 |
MPV (fL) | H | 7.2 ± 0.1 | 7.8 ± 0.6 | 8.0 ± 0.5 |
L | 7.3 ± 0.1 | 7.9 ± 0.4 | 8.1 ± 0.3 |
C | 6.9 ± 0.5 | 8.1 ± 0.5 | 7.6 ± 0.5 |
HGB (g/L) | H | 189.7 ± 5.0 | 176.3 ± 4.5 | 183.0 ± 1.0 |
L | 170.0 ± 9.6 | 149.7 ± 8.1 | 156.0 ± 15.6 |
C | 160.7 ± 14.2 | 158.0 ± 24.5 | 152.0 ± 24.8 |
PDW | H | 16.5 ± 0.1 | 16.6 ± 0.3 | 16.6 ± 0.2 |
L | 16.8 ± 0.5 | 16.3 ± 0.2 | 16.3 ± 0.2 |
C | 16.6 ± 0.1 | 16.3 ± 0.2 | 16.2 ± 0.2 |
PLT (109/L) | H | 410.0 ± 76.3 | 367.0 ± 60.9 | 287.7 ± 27.1 |
L | 331.7 ± 27.7 | 440.3 ± 67.3 | 372.7 ± 61.2 |
C | 418.0 ± 25.0 | 459.7 ± 24.0 | 377.7 ± 51.9 |
PCT (%) | H | 0.3 ± 0.1 | 0.3 ± 0.0 | 0.2 ± 0.0 |
L | 0.2 ± 0.1 | 0.4 ± 0.1 | 0.3 ± 0.1 |
C | 0.2 ± 0.1 | 0.4 ± 0.0 | 0.3 ± 0.1 |
Gran (109/L) | H | 3.8 ± 0.7 | 5.6 ± 4.6 | 2.9 ± 1.4 |
L | 2.9 ± 0.2 | 4.4 ± 2.0 | 2.2 ± 1.3 |
C | 2.4 ± 0.8 | 4.6 ± 1.5 | 2.7 ± 0.7 |
Gran (%) | H | 71.3 ± 7.1 | 63.9 ± 6.6 | 58.1 ± 12.6 |
L | 72.8 ± 8.2 | 71.0 ± 7.7 | 60.0 ± 7.5 |
C | 70.3 ± 14.0 | 69.6 ± 12.5 | 64.5 ± 8.4 |
Lymphocyte phenotyping by flow cytometry
Peripheral blood lymphocyte subset analyses were performed in a FACSCalibur flow cytometer (BD, Franklin Lakes, NJ, USA) using a panel of mouse anti-human monoclonal antibodies known to cross-react with macaque receptors. Staining was performed on whole blood preparations. The lymphocyte subsets were stained for CD3 (PE; clone SP34; BD), CD4 (PerCP; clone L200; BD), and CD8 (FITC; clone RPA-T8; BD). The T cell subset counts in the peripheral blood were determined by the TruCount™ method (BD, San Jose, CA, USA) using the FACSCalibur flow cytometer. The CD4+ and CD8+ T cell counts were reported as cell number/microliter.
Viral load measurement
Plasma samples were analyzed for viral RNA (vRNA) by real-time quantitative RT-PCR assays as described previously [
8]. Briefly, vRNA was extracted with a High Pure Viral RNA Kit (Roche, Mannheim, Germany) in accordance with the manufacturer’s instructions. A two-step RT-qPCR assay using a PrimeScript™ RT Reagent Kit and Premix ExTaq™ (Takara, Dalian, China) was performed in a 7500 Fast Real-Time PCR System (Applied Biosystems, Foster City, CA, USA). Each sample was tested in triplicate. Viral loads were reported as vRNA copy numbers per milliliter of plasma. The detection limit of the assay was 100 vRNA copies/mL.
Statistical analysis
Statistical analyses were performed using SPSS software 21.0 (SPSS Inc., Chicago, IL, USA) and GraphPad Prism version 6.0 (GraphPad Inc., San Diego, CA, USA). An independent-samples t-test was used for comparisons of differences in CD4+ T cell counts and plasma viral loads between two independent groups. A paired-samples t-test was used to compare CD4+ T cell counts and plasma viral loads between different time points within the same group. Spearman’s correlation analysis was used to assess the relationships between CD4/CD8 ratio and CD4+ T cell count, CD8+ T cell count, or plasma vRNA level. Values of P < 0.05 were considered statistically significant.
Discussion
The present study analyzed the effects of AKQ administration on viral loads, CD4
+ T cell counts, and CD8
+ T cell counts in SHIV89.6-infected Ch-RMs. To our knowledge, this is the first attempt to study the effect of a Chinese medicine in SHIV89.6-infected Ch-RMs. Ch-RMs develop AIDS-like symptoms more slowly than Indian macaques when exposed to SIV or SHIV [
10]. Mothé et al. [
11] reported Ch-RM MHC immunogenetics are more similar to HLA than those of Indian macaques, and therefore that Ch-RMs might be a better model for HIV. The SIV-infected Ch-RM has been successfully used as a model for studying responses to combination antiretroviral therapy (ART) and evaluating candidate eradication strategies to cure HIV infection [
12]. Our study was performed to develop a chronically SHIV89.6-infected Ch-RM model for detailed investigation of Chinese medicine therapeutic effects. High-dose AKQ therapy reduced the viral loads in SHIV89.6-infected Ch-RMs when initiated early after infection, thereby preventing the immunologic damage caused by HIV-1. AKQ treatment showed a beneficial effect on T cell recovery in the SHIV89.6-infected animals in accordance with previous findings in a clinical study [
5].
In untreated HIV-infected patients, the CD4/CD8 ratio can be used not only as a predictor of poor prognosis [
13], but also as a predictor of immune restoration [
14] and AIDS-related morbidities. Serrano-Villar et al. [
9] reported that patients with early initiation of ART were more likely to achieve a higher CD4/CD8 ratio than patients with later initiation of ART (2 years after infection). To our knowledge, no studies have specifically addressed the clinical significance of the CD4/CD8 ratio in SHIV-infected Ch-RMs on therapy. In our study, the animals in the high-dose group displayed a CD4/CD8 ratio increase from their baseline level before AKQ initiation. Meanwhile, a significant increase in the CD4/CD8 ratio failed to appear because the increase in CD4
+ T cells was accompanied by a simultaneous increase in CD8
+ T cells. In the untreated animals, the CD4/CD8 ratio showed strong correlations with the CD8
+ T cell count and plasma vRNA level, but not with the CD4
+ T cell count. Remarkably, the associated relationships changed and only the CD4
+ T cell count was positively correlated with the CD4/CD8 ratio in the high-dose group after treatment. We assumed that the CD4/CD8 ratio was essentially dependent on the CD4
+ T cell count in the animals with successful CD4
+ T cell recovery. Helleberg et al. [
15] reported that a major decline in the CD4
+ T cell count was associated with markedly increased risks of cardiovascular disease, cancer, and death among ART-treated HIV patients. Takuva et al. [
16] reported that patients on ART with poor CD4
+ T cell recovery during early treatment were at greater risk of progression to new AIDS diagnosis or death despite viral suppression.
Baicalein and baicalin, isolated from
Scutellaria baicalensis Georgi, were shown to be potent inhibitors of integrase and reverse transcriptase from HIV-1 [
17]. Liu et al. [
18] reported that crude extracts from Cortex
Phellodendri exhibited antifungal activities in vitro, and suggested their use for treatment of candidiasis in HIV/AIDS patients. Tang et al. [
19] reported that a crude extract of
Rhizoma Polygoni Cuspidati inhibited HIV-1 reverse transcriptase. Abd-Elazem et al. [
20] reported that water-soluble extracts of
Salvia miltiorrhiza Bge. inhibited HIV-1 integrase activities. All of these findings suggest that AKQ may suppress viral replication at multiple steps in the life cycle of HIV-1.
Many people living with HIV/AIDS in China are using complementary medicine [
21]. In 1996, a randomized trial tested a Chinese herbal formulation composed of 31 Chinese herbs in 30 HIV patients for treatment of HIV-related symptoms for a duration of 12 weeks. The study found that the symptoms were reduced in patients receiving the herbal formulation, but not in those receiving the placebo [
22]. However, no significant differences were found between the two groups in a follow-up study [
23]. A recent study showed that indirubin, the active ingredient of the Chinese herbal formula
Dan Gui Long Hui Wan, suppressed viremia of multidrug-resistant HIV molecular clones in animal models [
24]. HAART for HIV/AIDS is currently limited by the inability to eliminate the latent viral reservoir. The goal of HIV therapy is immune control of virus replication, rather than eradication. A combination of anti-inflammatory, antiretroviral, and immunological therapies might lead to total viral suppression and restoration of immune function in AIDS patients [
25,
26]. AKQ at an appropriate concentration (1.65 g/kg) decreased the plasma viral loads in SHIV89.6 chronically-infected Ch-RMs. AKQ was effective in preventing the decline of circulating CD4
+ T cells. The largest increase in CD4
+ T cells after treatment was observed in the high-dose group, which corresponded well with the significant decrease in the SHIV89.6 viral loads in this group.
One possible limitation of the present study was the small number of animals analyzed in each group. In accordance with the 3R (replacement, reduction, and refinement) principles [
27], we used three Ch-RMs per group in an 8-week test for AKQ treatment. To minimize the experimental variables, we carefully controlled some animal characteristics, such as age and weight, in our study.
Authors’ contributions
LCF, YJH and YTZ conceived the study and designed the experiments. GHZ, JBH, RHL, and XC performed AKQ treatment experiments and collected the blood samples. XHZ carried out lymphocyte phenotyping studies. LZ performed the viral load test. GHZ and YTZ interpreted the experimental results and wrote the manuscript. All authors read and approved the final manuscript.