Human Papillomavirus (HPV) – Cannabis Research

Human Papillomavirus (HPV) Research Dashboard

1

Primary Studies

7

Related Studies

8

Total Studies

Clinical Studies

0

Clinical Meta-analyses

0

Double-blind Clinical Trials

0

Clinical Trials

Pre-Clinical Studies

0

Meta-analyses/Reviews

1

Animal Studies

0

Laboratory Studies

What am I missing as a non-subscriber?

To see a full dashboard with study details and filtering, go to our DEMO page.

As a subscriber, you will be able to access dashboard insights including chemotype overviews and dosing summaries for medical conditions and organ system and receptor breakdowns for cannabinoid and terpene searches. Study lists present important guidance including dosing and chemotype information with the ability to drill down to the published material. And all outputs are fully filterable, to help find just the information you need. Stay up-to-date with the science of cannabis and the endocannabinoid system with CannaKeys.

CannaKeys has 8 studies associated with Human Papillomavirus (HPV).

Here is a small sampling of Human Papillomavirus (HPV) studies by title:


Components of the Human Papillomavirus (HPV) Research Dashboard

  • Dosing information available for Human Papillomavirus (HPV)
  • Chemotype guidance for treating Human Papillomavirus (HPV) with cannabis
  • Synopsis of cannabis research for Human Papillomavirus (HPV)
  • Individual study details for Human Papillomavirus (HPV)

Ready to become a subscriber? Go to our PRICING page.

Human Papillomavirus (HPV) Research Dashboard

1

Primary Studies

7

Related Studies

8

Total Studies

Clinical Studies

0

Clinical Meta-analyses

0

Double-blind Clinical Trials

0

Clinical Trials

Pre-Clinical Studies

0

Meta-analyses/Reviews

1

Animal Studies

0

Laboratory Studies

What am I missing as a non-subscriber?

To see a full dashboard with study details and filtering, go to our DEMO page.

As a subscriber, you will be able to access dashboard insights including chemotype overviews and dosing summaries for medical conditions and organ system and receptor breakdowns for cannabinoid and terpene searches. Study lists present important guidance including dosing and chemotype information with the ability to drill down to the published material. And all outputs are fully filterable, to help find just the information you need. Stay up-to-date with the science of cannabis and the endocannabinoid system with CannaKeys.

CannaKeys has 8 studies associated with Human Papillomavirus (HPV).

Here is a small sampling of Human Papillomavirus (HPV) studies by title:


Components of the Human Papillomavirus (HPV) Research Dashboard

  • Dosing information available for Human Papillomavirus (HPV)
  • Chemotype guidance for treating Human Papillomavirus (HPV) with cannabis
  • Synopsis of cannabis research for Human Papillomavirus (HPV)
  • Individual study details for Human Papillomavirus (HPV)

Ready to become a subscriber? Go to our PRICING page.

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Overview - Human Papillomavirus (HPV)

Description of Human Papillomavirus (HPV)

Human papillomavirus (HPV) is one of the most common viral infections worldwide, with over 200 known types that primarily infect epithelial tissues of the skin and mucous membranes. Transmission occurs mainly through direct skin-to-skin or sexual contact. While most HPV infections are transient and cleared by the immune system within one to two years, certain strains can persist and lead to disease.


HPV types are generally categorized into low-risk and high-risk groups:



  • Low-risk HPV types (such as HPV-6 and HPV-11) are not associated with cancer but can cause benign growths. The most common are anogenital warts (condylomata acuminata) and recurrent respiratory papillomatosis, a rare condition where warts grow in the respiratory tract, sometimes obstructing airflow.

  • High-risk HPV types (particularly HPV-16 and HPV-18, but also several others like 31, 33, and 45) are strongly linked to the development of cancers. These viruses can integrate into host cell DNA, disrupting normal cell-cycle regulation and leading to uncontrolled growth.


The most significant conditions caused by persistent high-risk HPV infection include:



  • Cervical cancer – nearly all cases are attributable to HPV, making it the leading HPV-related malignancy worldwide.

  • Other anogenital cancers – HPV is implicated in cancers of the vulva, vagina, penis, and anus.

  • Oropharyngeal cancers – particularly cancers of the tonsils and base of tongue, which have been rising in incidence, especially in men.


Importantly, HPV infection is often asymptomatic, meaning individuals may unknowingly transmit the virus. Preventive strategies are therefore crucial. Regular cervical screening (Pap tests, HPV testing) remains a cornerstone in reducing cancer incidence and mortality, as early detection of precancerous changes allows for effective intervention.


HPV vaccination has been in the news recently, sparking debate between proponents and critics. Advocates point to robust evidence of reduced HPV infections, precancerous lesions, and related cancers in populations with high vaccination rates. Opponents, meanwhile, raise concerns about potential side effects, long-term safety data, and the balance of individual choice versus public health goals. Both sides draw on scientific studies and expert commentary, underscoring the ongoing need for transparent communication and continued research.

Disease Classification

Condition: Human Papillomavirus (HPV)
Disease Family:
Organ System: Reproductive System
ICD-10 Chapter: Certain infectious and parasitic diseases
ICD-10 Code: B97.7

Human Papillomavirus (HPV) Symptoms:

Most HPV infections are asymptomatic and clear on their own within 1–2 years, but when symptoms occur, they depend on the HPV type (low-risk vs. high-risk). Common symptoms of HPV infection: Genital warts [small, flesh-colored or gray growths in the genital or anal area; may be flat, raised, or cauliflower-like clusters (caused mainly by HPV types 6 & 11)]. Respiratory papillomatosis (rare): Warts in the respiratory tract that can cause hoarseness, breathing difficulties, or airway obstruction. Symptoms linked to high-risk HPV (persistent infection): Precancerous cervical changes (detected via Pap smear or HPV test, usually asymptomatic at first). Abnormal vaginal bleeding (e.g., after intercourse, between periods, or after menopause). Pelvic pain or discomfort (less common, may indicate advanced disease). Other cancer-related symptoms depending on site (anal, penile, vulvar, vaginal, or oropharyngeal cancers)—often not apparent until later stages.

Also known as:

HPV, Papillomavirus, Human wart virus, Genital wart virus, Oncogenic papillomavirus,

Drug Interactions

THC Interaction with Pharmaceutical Drugs

  • Tetrahydrocannabinol (THC) can enhance the effects of drugs that cause sedation and depress the central nervous system, such as benzodiazepines, barbiturates, and alcohol. 
  • THC is metabolized by an inhibitor of several enzymatic liver pathways referred to as cytochrome P450 (aka CYP450). There are more than 50 enzymes belonging to this enzyme family, several of which are responsible for the breakdown of common drugs such as antidepressants (e.g., amitriptyline, doxepin, fluvoxamine), antipsychotics (haloperidol, clozapine, Stelazine), beta-blockers (e.g., propranolol), bronchodilators (e.g., theophylline), or blood thinners (e.g., warfarin). Thus, patients taking these medication classes may find that THC increases the concentration and effects of these drugs and the impact duration.
  • Clinical observation (not yet confirmed by clinical trials) suggests no likely interactions with other pharmaceuticals at a total daily dose of up to 20mg THC.

If you are interested in the interaction potential of specific pharmaceuticals with THC, consider visiting these free drug interaction checkers: Drugs.com or DrugBank Online.

CBD Interaction with Pharmaceutical Drugs

  • Cannabidiol (CBD) may alter the action of metabolic enzymes (specific drug-transport mechanisms) and alter interactions with other drugs, some of which may produce therapeutic or adverse effects. For instance, CBD interacts with the enzyme cytochrome P450 3A4 and cytochrome P450 2C19, increasing the bioavailability of anti-epileptic drugs such as clobazam (a benzodiazepine). This makes it possible to achieve the same results at significantly lower dosages, reducing treatment costs and risks of adverse effects. 
  • Groups of drugs affected include anti-epileptics, psychiatric drugs, and drugs affecting metabolic enzymes.
  • Clinical observations (not yet confirmed by clinical trials) suggest no likely interactions with other pharmaceuticals at a total daily dose of up to 100mg CBD.

If you are interested in the interaction potential of specific pharmaceuticals with CBD, consider visiting these free drug interaction checkers: Drugs.com or DrugBank Online.

THC/CBD Interaction with Pharmaceutical Drugs

In general, when using cannabinoid-based therapeutics that contain both THC and CBD consider the ratio between them and weigh the relevant information displayed in the individual THC and CBD Drug Interaction windows accordingly.

If you are interested in the interaction potential of specific pharmaceuticals with both primary cannabinoids and THC/CBD, consider visiting these free drug interaction checkers: Drugs.com or DrugBank Online.

Concerns about Cannabis and Cancer-related Immunotherapies:
Some recent clinical observational studies have suggested that the co-administration of cannabinoid-based therapeutics and immunotherapy or immune checkpoint inhibitors in the treatment of certain types of cancer has been associated with worse overall survival rates (T. Taha et al., 2019; A. Biedny et al., 2020; G. Bar-Sela et al., 2020).

However, other studies have suggested that the co-commitment use of immune checkpoint inhibitors and cannabis-induced no such deleterious effects. More specifically, one trial was conducted on animals resulting in data suggesting that cannabis did not negatively affect the properties of immune checkpoint inhibitors (B. Waissengrin et al., 2023). The same authors compared the previous study results with findings from a cohort of 201 patients with metastatic non-small cell lung cancer who received treatment with monotherapy pembrolizumab as a first-line treatment and adjunct cannabis to treat mainly pain and loss of appetite. Their time to tumor progression was 6.1 versus 5.6 months, and overall survival differed between 54.9 versus 23.6 months in cannabis-naïve patients and cannabis-using patients, respectively. However, while numerically different, the authors write that these differences were not statistically significant, leading them to suggest that “These data provide reassurance regarding the absence of a deleterious effect of cannabis in this clinical setting.”

Dosing Considerations

THC Dosage Considerations

  • THC micro dose:  0.1 mg to 0.4 mg
  • THC low dose:  0.5 mg to 5 mg
  • THC medium dose:  6 mg to 20 mg
  • THC high dose:  21 mg to 50+ mg

CBD Dosage Considerations

  • CBD low dose:  0.4 mg to 19 mg
  • CBD medium dose: 20 mg to 99 mg
  • CBD high dose:  100 mg to 800+ mg (upper limits tested ~1,500mg)
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Disclaimer
Information on this site is provided for informational purposes only and is not meant to substitute for the advice provided by your own licensed physician or other medical professional. You should not use the information contained herein for diagnosing or treating a health problem or disease. If using a product, you should read carefully all product packaging. If you have or suspect that you have a medical problem, promptly contact your health care provider.

Information on this site is based on scientific studies (human, animal, or in vitro), clinical experience, or traditional usage as cited in each article. The results reported may not necessarily occur in all individuals. For many of the conditions discussed, treatment with prescription or over-the-counter medication is also available. Consult your physician, nutritionally oriented health care practitioner, and/or pharmacist for any health problem and before using any supplements or before making any changes in prescribed medications.